Pivalic acid → ethyl (S)(E)-2-{2-[2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetate

HRID 1757214

반응식

HRID 1757214 반응식
[Si:1]([O:8][C:9]1[C:17]([CH2:18][C@@H:19]([C:21]2[CH2:25][CH2:24][CH2:23][CH:22]=2)O)=[C:16]([CH2:26][CH3:27])[C:15]([CH3:28])=[C:14]2[C:10]=1[C:11](=[O:29])[O:12][CH2:13]2)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].C(O)(=O)C(C)(C)C.[C:37](OCC)([O:42]CC)([O:39][CH2:40][CH3:41])[CH3:38]>>[Si:1]([O:8][C:9]1[C:17]([CH2:18]/[CH:19]=[C:21]2/[C@H:22]([CH2:38][C:37]([O:39][CH2:40][CH3:41])=[O:42])[CH2:23][CH2:24][CH2:25]/2)=[C:16]([CH2:26][CH3:27])[C:15]([CH3:28])=[C:14]2[C:10]=1[C:11](=[O:29])[O:12][CH2:13]2)([C:4]([CH3:5])([CH3:6])[CH3:7])([CH3:2])[CH3:3]

참가 물질

4

반응 조건

온도
138 °C

실험 절차

A mixture of (S)-2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-cyclopentenyl-1-hydroxyethane (2.8 g), pivalic acid (0.1 g) and triethyl orthoacetate (125 ml) was heated to 138° C. After 2.5 hours, more pivalic acid (65 mg) was added and the reaction was continued 1 hour more. The reaction mixture was cooled, the excess triethyl orthoacetate removed in vacuo, and the residue chromatographed on silica gel (20% ethyl acetate/hexane) to give ethyl (S)(E)-2-{2-[2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetate.

후처리

  1. waitthe reaction was continued 1 hour
  2. temperatureThe reaction mixture was cooled
  3. customthe excess triethyl orthoacetate removed in vacuo
  4. customthe residue chromatographed on silica gel (20% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-8ded6eb85cec47719debcd81f0ca80d8
출처 데이터셋
uspto-grants-1995_08
특허 번호
US05444072

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