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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 19378100, 화합물 → HCID 19378071, 화합물

HRID 2211017
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HRID 2211017 반응식
[SH:1][C:2]([CH:5]1[O:10][C:8](=[O:9])[CH:7]([CH2:11][SH:12])[CH2:6]1)([CH3:4])[CH3:3]>C(Cl)Cl.C(Br)C=C.CCOCC>[CH2:4]([S:1][C:2]([CH:5]1[O:10][C:8](=[O:9])[CH:7]([CH2:11][S:12][CH2:7][CH:6]=[CH2:5])[CH2:6]1)([CH3:4])[CH3:3])[CH:2]=[CH2:3]
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참가 물질

5

반응물 1

HCID 19378100HCID 19378100, 화합물

생성물 1

HCID 19378071HCID 19378071, 화합물

시약·촉매·용매 3

HCID 3283Diethyl Ether용매HCID 6344Dichloromethane용매HCID 7841Allyl bromide용매

실험 절차

To a solution of 4-(1-mercapto-1-methylethyl)-2-mercaptomethyl-4-butanolide (0.24 g) in methylene chloride (3 ml), allyl bromide (1.0 ml) and N,N-(diisopropyl)ethylamine (1.0 ml) were added under nitrogen atmosphere. The mixture was stirred overnight at room temperature. The mixture was diluted with ether (50 ml) and washed with 2N hydrochloric acid and saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The oily residue was purified by silica gel column chromatography to give 0.142 g (43%) of cis-form (compound No.12-1) and 0.170 g (51%) of transform (compound No.12-2) of the titled compound.

후처리

  1. washwashed with 2N hydrochloric acid and saturated sodium chloride solution
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. concentrationconcentrated in vacuo
  4. customThe oily residue was purified by silica gel column chromatography
  5. customto give 0.142 g (43%) of cis-form (compound No.12-1) and 0.170 g (51%)

출처 및 근거

ORD 기록
ord-db584e54c3a94e1195a26356a8ac06f4
출처 데이터셋
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05461158

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