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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium borohydride → (3-Bromo-5-chloropyridin-4-yl)methanol

HRID 1897595
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HRID 1897595 반응식
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:10])[C:7]=1[CH:8]=[O:9].[BH4-].[Na+]>C1COCC1.O.C(Cl)Cl>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:10])[C:7]=1[CH2:8][OH:9]
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참가 물질

6

반응물 2

HCID 4311764Sodium borohydrideHCID 730126133-Bromo-5-chloropyridine-4-carboxaldehyde

생성물 1

HCID 44190471(3-Bromo-5-chloropyridin-4-yl)methanol수율 98.7%

시약·촉매·용매 3

HCID 962Water용매HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매

실험 절차

To the solution of 3-Bromo-5-chloro-pyridine-4-carbaldehyde (270 mg, 1.23 mmol) in THF (5 mL) and water (1 mL) was added NaBH4 (139 mg, 3.67 mmol). The resulting mixture was stirred for another 1 h, and was diluted with DCM. The organic layer was washed with water and brine. The aqueous layer was extracted with DCM. The combined extracts were separated and concentrated in vacuo to give 270 mg of title compound without further purification. ESI-MS m/z: 223.9 [M+1]+, Retention time 1.01 min. 1H-NMR (CDCl3, 400 MHz) δ 4.88 (s, 2H), 8.46 (s, 1H), 8.56 (s, 1H).

후처리

  1. washThe organic layer was washed with water and brine
  2. extractionThe aqueous layer was extracted with DCM
  3. customThe combined extracts were separated
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2ea079a706e54866b11fb4b926c42829
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08519134B2

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