반응식
[Si:1]([O:8][CH2:9][C:10]1[CH:11]=[C:12]([OH:16])[CH:13]=[CH:14][CH:15]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].ClC(Cl)(O[C:21](=[O:27])[O:22][C:23](Cl)(Cl)Cl)Cl.N1C=CC=CC=1.[CH3:35][S:36]([C:39]1[CH:44]=[CH:43][C:42](/[C:45](=[C:48](\[C:51]2[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=2)/[CH2:49][OH:50])/CO)=[CH:41][CH:40]=1)(=[O:38])=[O:37]>C(Cl)Cl>[C:21](=[O:27])([O:22][CH2:23]/[C:45](/[C:42]1[CH:41]=[CH:40][C:39]([S:36]([CH3:35])(=[O:38])=[O:37])=[CH:44][CH:43]=1)=[C:48](/[C:51]1[CH:52]=[CH:53][CH:54]=[CH:55][CH:56]=1)\[CH2:49][OH:50])[O:16][C:12]1[CH:13]=[CH:14][CH:15]=[C:10]([CH2:9][O:8][Si:1]([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2])[CH:11]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 3.06 g of 3-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenol and 1.50 g of triphosgene in 20 mL of CH2Cl2 cooled at −78° C. was added 1.2 mL of pyridine. The reaction mixture was warmed to rt. After 15–30 min, the white suspension was transferred to a solution containing 5.95 g of (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol and 1.5 mL of pyridine in 20 mL of CH2Cl2 at rt. The reaction was stirred at rt for 15 min. The reaction was quenched with aqueous 1N HCl, extracted with EtOAc and washed with brine, dried over sodium sulfate, evaporated, and purified by flash chromatography (50–70% EtOAc/hexane) to afford 1.26 g of the title compound as a yellow oil.
후처리
- waitAfter 15–30 min
- customThe reaction was quenched with aqueous 1N HCl
- extractionextracted with EtOAc
- washwashed with brine
- dry with materialdried over sodium sulfate
- customevaporated
- custompurified by flash chromatography (50–70% EtOAc/hexane)
출처 및 근거
- ORD 기록
- ord-6194b3a9f7d34c66af83ac79ba135f51
- 출처 데이터셋
- uspto-grants-2007_04
- 특허 번호
- US07199154B2
연결된 노트
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