Sodium borohydride → (4-Bromopyridin-2-yl)methanol

HRID 1895787

반응식

HRID 1895787 반응식
[BH4-].[Na+].C[O:4][C:5]([C:7]1[CH:12]=[C:11]([Br:13])[CH:10]=[CH:9][N:8]=1)=O>C(O)C>[Br:13][C:11]1[CH:10]=[CH:9][N:8]=[C:7]([CH2:5][OH:4])[CH:12]=1

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 12828947Methyl 4-bromopicolinate

생성물 1

HCID 14761462(4-Bromopyridin-2-yl)methanol수율 94%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Sodium borohydride (763 mg, 20.17 mmol) was added portionwise to a solution of 4-bromo-pyridine-2-carboxylic acid methyl ester (1.98 g, 9.166 mmol) in ethanol (50 mL) under nitrogen and the reaction mixture was stirred at room temperature for 18 hours. The reaction was quenched by the addition of acetone (10 mL) and the reaction was stirred for 15 minutes. The solvent was evaporated and the residue partitioned between water and ethyl acetate. The aqueous layer was extracted with ethyl acetate and the combined organics were collected, dried over anhydrous sodium sulfate and the solvent evaporated to afford the title compound (1.61 g, 94%) as a yellow oil. 1H NMR (300 MHz, CDCl3) δ3.4-3.5 (br s, 1H), 4.80 (s, 2H), 7.40 (dd, J=5.4, 1.8 Hz, 1H), 7.50 (br m, 1H), 8.39 (d, J=5.4 Hz, 1H). LCMS (m/z) 188/200 [M+H], Tr=1.55 min.

후처리

  1. customThe reaction was quenched by the addition of acetone (10 mL)
  2. stirringthe reaction was stirred for 15 minutes
  3. customThe solvent was evaporated
  4. customthe residue partitioned between water and ethyl acetate
  5. extractionThe aqueous layer was extracted with ethyl acetate
  6. customthe combined organics were collected
  7. dry with materialdried over anhydrous sodium sulfate
  8. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-15ffff39da5646a7a92fcc78b1955d75
출처 데이터셋
uspto-grants-2013_08
특허 번호
US08513184B2

연결된 노트

불러오는 중…