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Sodium borohydride → 2-Cyano-5-hydroxymethylpyridine

HRID 571693
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인쇄 미리보기

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HRID 571693 반응식
[CH:1]([C:3]1[CH:4]=[CH:5][C:6]([C:9]#[N:10])=[N:7][CH:8]=1)=[O:2].[BH4-].[Na+]>CO>[OH:2][CH2:1][C:3]1[CH:4]=[CH:5][C:6]([C:9]#[N:10])=[N:7][CH:8]=1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 109862635-Formylpyridine-2-carbonitrile

생성물 1

HCID 122519662-Cyano-5-hydroxymethylpyridine수율 86.6%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
0 °C

실험 절차

To a 0° C. solution of 5-formylpicolinonitrile (490 mg, 3.71 mmol) in 15 mL of MeOH was added NaBH4 (140 mg, 3.71 mmol). The reaction mixture was stirred at 0° C. for 1 h and quenched with 5% citric acid. After most MeOH was removed by concentration, the residue was partitioned between DCM and sat. NaHCO3 (aq.). The aqueous layer was extracted with DCM (10×). The organic layer was washed with brine and dried (Na2SO4). The product 5-(hydroxymethyl)picolinonitrile (431 mg) was obtained by concentration under vacuum.

후처리

  1. customquenched with 5% citric acid
  2. customAfter most MeOH was removed by concentration
  3. customthe residue was partitioned between DCM and sat. NaHCO3 (aq.)
  4. extractionThe aqueous layer was extracted with DCM (10×)
  5. washThe organic layer was washed with brine
  6. dry with materialdried (Na2SO4)

출처 및 근거

ORD 기록
ord-798301b99eac48ad837b69b0a2095869
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029362B2

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