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Methanol → HCID 20448815, 화합물

HRID 358375
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HRID 358375 반응식
[Si:1]([O:8][CH:9]1[CH2:13][C:12](=O)[CH:11]2[O:15][CH:10]12)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].O[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][SH:22].C(N(CC)CC)C.[CH3:30][OH:31]>>[Si:1]([O:8][CH:9]1[CH2:10][C:11](=[O:15])[C:12]([S:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:30][OH:31])=[CH:13]1)([C:4]([CH3:5])([CH3:6])[CH3:7])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 887MethanolHCID 8471TriethylamineHCID 5342595-Mercapto-1-pentanolHCID 133625094(RS)-t-butyldimethylsilyloxy-2,3-epoxycyclopentanone

생성물 1

HCID 20448815HCID 20448815, 화합물수율 31%

실험 절차

1.26 g (5.94 mmoles) of 4(RS)-t-butyldimethylsilyloxy-2,3-epoxy cyclopentanone and 804 mg (6.0 mmoles) of 5-hydroxy-1-pentanethiol were dissolved in 10 ml of methanol, and 606 mg (6 mmoles) of triethylamine was added. After the reaction was carried out for 10 minutes, the solvent was evaporated to give 2.1 g of a crude product. The crude product was subjected to dry column chromatography and developed with hexane/ethyl acetate (7/3) to give 710 mg (2.16 mmoles; yield 31%) of 4-t-butyldimethylsilyloxy-2-(6-hydroxyhexylthio)-2-cyclopentenone.

후처리

  1. customthe solvent was evaporated
  2. customto give 2.1 g of a crude product
  3. customto dry column chromatography

출처 및 근거

ORD 기록
ord-7314d9bdce254358b3ff22a3cf58e4e3
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04466980

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