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Triethylamine → (2-Bromopyridin-3-yl)methanol

HRID 1471684
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HRID 1471684 반응식
[Br:1][C:2]1[N:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].C(N(CC)CC)C.ClC(OCC(C)C)=O.[BH4-].[Na+]>C1COCC1.O>[Br:1][C:2]1[C:3]([CH2:4][OH:5])=[CH:7][CH:8]=[CH:9][N:10]=1
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참가 물질

7

반응물 4

HCID 8471TriethylamineHCID 62365Isobutyl chloroformateHCID 2332622-Bromopyridine-3-carboxylic acidHCID 4311764Sodium borohydride

생성물 1

HCID 14761460(2-Bromopyridin-3-yl)methanol수율 90.4%

시약·촉매·용매 2

HCID 962Water용매2회
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 8028
Tetrahydrofuran
용매

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온도
0 °C

실험 절차

To a solution of 2-bromonicotinic acid (4.0 g, 20 mmol) and triethylamine (3.34 mL, 24 mmol, 1.2 eq.) in THF (100 mL) was added i-butyl chloroformate (3.12 mL, 24 mmol, 1.2 eq.) at 0° C. The mixture was stirred at 0° C. for 10 min and filtered. To this filtrate was added a suspension of NaBH4 (1.52 g, 40 mmol, 2 eq.) in water (1.0 mL) at 0° C. The mixture was stirred for 30 min, added water (3 mL), continued to stir for 2 h, and concentrated to dryness. The crude was purified on silica gel using a mixture of ethylacetate and hexanes as eluent to give (2-bromopyridin-3-yl)methanol (3.4 g, 90%) as a white solid. LRMS (M+H+) m/z 188.0.

후처리

  1. filtrationfiltered
  2. additionTo this filtrate was added
  3. stirringThe mixture was stirred for 30 min
  4. stirringto stir for 2 h
  5. concentrationconcentrated to dryness
  6. customThe crude was purified on silica gel using
  7. additiona mixture of ethylacetate and hexanes as eluent

출처 및 근거

ORD 기록
ord-59d4aba445a24dea945ac52eadd613ae
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012450B2

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