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Triethylamine → (S)-2-Methyl-3-(3-methyl-5-vinyl-phenylmethanesulfonyl)-propionic acid

HRID 1432104
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HRID 1432104 반응식
[CH:1]([B-](F)(F)F)=[CH2:2].[K+].C(N(CC)CC)C.Br[C:16]1[CH:17]=[C:18]([CH2:23][S:24]([CH2:27][C@@H:28]([CH3:32])[C:29]([OH:31])=[O:30])(=[O:26])=[O:25])[CH:19]=[C:20]([CH3:22])[CH:21]=1>C(O)CC.CCOC(C)=O>[CH3:32][C@H:28]([CH2:27][S:24]([CH2:23][C:18]1[CH:19]=[C:20]([CH:21]=[CH2:16])[CH:22]=[C:1]([CH3:2])[CH:17]=1)(=[O:25])=[O:26])[C:29]([OH:31])=[O:30]
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반응물 3

HCID 8471TriethylamineHCID 23679353Potassium vinyltrifluoroborateHCID 68544363(S)-3-(3-bromo-5-methyl-phenylmethanesulfonyl)-2-methyl-propionic acid

생성물 1

HCID 68541338(S)-2-Methyl-3-(3-methyl-5-vinyl-phenylmethanesulfonyl)-propionic acid

시약·촉매·용매 2

HCID 10311-Propanol용매
HCID 8857
Ethyl Acetate
용매

실험 절차

Potassium vinyltrifluoroborate (247 mg, 1.8 mmol), triethylamine (0.21 ml, 1.5 mmol) and [1,1′-bis(diphenylphosphino-κP)ferrocene]dichloro-palladium (24 mg) are added to (S)-3-(3-bromo-5-methyl-phenylmethanesulfonyl)-2-methyl-propionic acid (0.5 g, 1.5 mmol) in 25 ml propanol. The mixture is stirred under argon for 2.5 hrs at reflux. After cooling to rt the mixture is diluted with EtOAc, washed with 0.5 N aqueous hydrochloric acid and brine, dried over magnesium sulfate, and the solvents are evaporated. The residue is purified by chromatography on silica gel (flashmaster, DCM to DCM/methanol 9/1) followed by crystallization from DCM/diethyl ether/hexane to give the title compound as off-white crystals.

후처리

  1. temperatureat reflux
  2. washwashed with 0.5 N aqueous hydrochloric acid and brine
  3. dry with materialdried over magnesium sulfate
  4. customthe solvents are evaporated
  5. customThe residue is purified by chromatography on silica gel (flashmaster, DCM to DCM/methanol 9/1)
  6. customfollowed by crystallization from DCM/diethyl ether/hexane

출처 및 근거

ORD 기록
ord-264b5b54b65b45ef9759429cfbba757d
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07612055B2

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