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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium borohydride → 5-{3-[(1R,2R,3R,5R)-5-Chloro-2-((E)-3-hydroxy-oct-1-enyl)-3-(tetrahydro-pyran-2-yloxy)-cyclopentyl]-propyl}-thiophene-2-carboxylic acid methyl ester

HRID 1470679
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HRID 1470679 반응식
[BH4-].[Na+].[CH3:3][O:4][C:5]([C:7]1[S:8][C:9]([CH2:12][CH2:13][CH2:14][C@H:15]2[C@H:19]([Cl:20])[CH2:18][C@@H:17]([O:21][CH:22]3[CH2:27][CH2:26][CH2:25][CH2:24][O:23]3)[C@@H:16]2/[CH:28]=[CH:29]/[C:30](=[O:36])[CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])=[CH:10][CH:11]=1)=[O:6]>CO>[CH3:3][O:4][C:5]([C:7]1[S:8][C:9]([CH2:12][CH2:13][CH2:14][C@H:15]2[C@H:19]([Cl:20])[CH2:18][C@@H:17]([O:21][CH:22]3[CH2:27][CH2:26][CH2:25][CH2:24][O:23]3)[C@@H:16]2/[CH:28]=[CH:29]/[CH:30]([OH:36])[CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])=[CH:10][CH:11]=1)=[O:6]
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 57692812HCID 57692812, 화합물

생성물 1

HCID 576928175-{3-[(1R,2R,3R,5R)-5-Chloro-2-((E)-3-hydroxy-oct-1-enyl)-3-(tetrahydro-pyran-2-yloxy)-cyclopentyl]-propyl}-thiophene-2-carboxylic acid methyl ester수율 80%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

NaBH4 (9.2 mg, 0.24 mmol) was added to a solution of ketone 4-3 (59 mg, 0.12 mmol) in methanol (1 mL). The reaction was stirred at room temperature for 2 h and then was quenched by addition of 5 mL 1 M HCl. The resulting mixture was extracted with CH2Cl2 and the combined CH2Cl2 solution was dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (ethyl acetate/hexanes) gave the title compound (48 mg, 80%).

후처리

  1. customwas quenched by addition of 5 mL 1 M HCl
  2. extractionThe resulting mixture was extracted with CH2Cl2
  3. dry with materialthe combined CH2Cl2 solution was dried (Na2SO4)
  4. filtrationfiltered
  5. customevaporated
  6. customPurification by flash chromatography on silica gel (ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-b13754997529450eb8e18adff6dffba1
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006464B2

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