Chemical intermediate

77383-17-6

  • Product Name:Difluoro-propenyl-oxy valeric acid tert-butyl ester
  • Molecular Formula:
  • Specifications:99%
  • Molecular Weight:279.217
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Product Details;

CasNo: 77383-17-6

Factory Export Top Purity Difluoro-propenyl-oxy valeric acid tert-butyl ester 77383-17-6 In Stock

  • Molecular Formula:C12H23BrO2
  • Molecular Weight:279.217

77383-17-6 Relevant articles

TARGET PROTEIN EED DEGRADATION-INDUCING DEGRADUCER, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING DISEASES RELATED TO EED, EZH2, OR PRC2, COMPRISING SAME AS ACTIVE INGREDIENT

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Paragraph 0860-0862, (2021/12/23)

The present invention relates to a targe...

MACROCYCLIC INHIBITORS OF PEPTIDYLARGININE DEIMINASES

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Page/Page column 259-260, (2021/11/06)

The present disclosure relates to novel ...

Fluorescence detection of metabolic activity of the fatty acid beta oxidation pathway in living cells

Kamoda, Koichiro,Kawagoe, Ryosuke,Matsunaga, Naoya,Ohdo, Shigehiro,Ojida, Akio,Tsuruta, Akito,Uchinomiya, Shohei

supporting information, p. 3023 - 3026 (2020/03/18)

Detection of metabolic activity in livin...

ESTROGEN RECEPTOR PROTEIN DEGRADERS

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Paragraph 0214-0215, (2020/07/21)

The present disclosure provides compound...

77383-17-6 Process route

8-bromooctanoic acid
17696-11-6

8-bromooctanoic acid

<i>tert</i>-butyl alcohol
75-65-0

tert-butyl alcohol

8-bromo-octanoic acid tert-butyl ester
77383-17-6

8-bromo-octanoic acid tert-butyl ester

Conditions
Conditions Yield
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 ℃; for 2.5h; Inert atmosphere;
tert-butyl alcohol; In dichloromethane; at 0 - 20 ℃;
99%
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 ℃; for 2.5h; Inert atmosphere;
tert-butyl alcohol; In dichloromethane; at 20 ℃; for 3.5h; Inert atmosphere;
96%
8-bromooctanoic acid; With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃; for 1.5h; Inert atmosphere;
tert-butyl alcohol; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere;
68%
With sulfuric acid; magnesium sulfate; In dichloromethane; at 20 ℃; for 18h;
65%
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 - 20 ℃; for 2h;
tert-butyl alcohol; In dichloromethane; at 20 ℃; for 12h;
65%
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 - 20 ℃; for 2h;
tert-butyl alcohol; In dichloromethane; at 20 ℃; for 12h;
65%
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 ℃; for 2.5h;
tert-butyl alcohol; In dichloromethane; at 0 - 20 ℃; for 3.5h;
60%
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 ℃; for 2.5h;
tert-butyl alcohol; In dichloromethane; at 0 - 20 ℃; for 3.5h;
60%
With di-tert-butyl dicarbonate; magnesium chloride; at 40 ℃; for 48h;
55%
8-bromooctanoic acid; With trifluoroacetic anhydride; In tetrahydrofuran; at -40 ℃; for 0.5h;
tert-butyl alcohol; In tetrahydrofuran; at -40 - 20 ℃; for 16h;
44%
With ethyl bromide; oxalyl dichloride; sodium bromide; Yield given. Multistep reaction; 1.) DMF, MeCN, -18 deg C, 40 min, 2.) MeCN, -18 deg C, 45 min, 3.) pyridine, -18 deg C, 0.5 h; -18 deg C to room temperature, 20 h;
With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 48h;
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 ℃; for 2.5h;
tert-butyl alcohol; In dichloromethane; at 0 - 20 ℃; for 3.5h;
8-bromooctanoic acid; With trifluoroacetic anhydride; In dichloromethane; at 0 ℃; for 2.5h;
tert-butyl alcohol; In dichloromethane; for 1h;
8-bromooctanoic acid
17696-11-6

8-bromooctanoic acid

di-<i>tert</i>-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

8-bromo-octanoic acid tert-butyl ester
77383-17-6

8-bromo-octanoic acid tert-butyl ester

Conditions
Conditions Yield
With dmap; In dichloromethane; tert-butyl alcohol; at 20 ℃; for 16h;
With dmap; In dichloromethane; tert-butyl alcohol; at 20 ℃; for 16h;

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