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Methyl chloroformate → (3-Chloropyrazin-2-yl)methanol

HRID 1471718
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HRID 1471718 반응식
[Cl:1][C:2]1[C:3]([C:8](O)=[O:9])=[N:4][CH:5]=[CH:6][N:7]=1.ClC(OC)=O.[BH4-].[Na+]>C1COCC1.O>[Cl:1][C:2]1[C:3]([CH2:8][OH:9])=[N:4][CH:5]=[CH:6][N:7]=1
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참가 물질

6

반응물 3

HCID 6586Methyl chloroformateHCID 15019003-Chloro-2-pyrazine-carboxylic acidHCID 4311764Sodium borohydride

생성물 1

HCID 40152213(3-Chloropyrazin-2-yl)methanol수율 22%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a solution of 3-chloropyrazine-2-carboxylic acid (2.0 g, 12.70 mmol, 1.0 eq.) and TEA (3.50 mL, 25.40 mmol, 2.0 eq.) in THF (50 mL) was added methyl chloroformate (1.2 mL, 15.20 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 (0.97 g, 25.40 mmol, 2 eq.) in water (1.0 mL) at 0° C. The mixture was stirred at 0° C. for 1 h, quenched with NH4Cl(aq) solution, and extracted with EtOAc twice. The combined organic layers were dried over Na2SO4, concentrated, and purified on silica gel using a mixture of EtOAc and hexanes as eluent to give (3-chloropyrazin-2-yl)methanol (400 mg, 22%) as a white solid. 1H NMR (400 MHz, MeOD) δ 8.58 (d, J=2.5 Hz, 1H), 8.38 (d, J=2.5 Hz, 1H), 4.84 (s, 2H). LRMS (M+H+) m/z 145.1.

후처리

  1. filtrationfiltered
  2. additionTo this filtrate was added
  3. stirringThe mixture was stirred at 0° C. for 1 h
  4. customquenched with NH4Cl(aq) solution
  5. extractionextracted with EtOAc twice
  6. dry with materialThe combined organic layers were dried over Na2SO4
  7. concentrationconcentrated
  8. custompurified on silica gel using
  9. additiona mixture of EtOAc and hexanes as eluent

출처 및 근거

ORD 기록
ord-2b11664989d24ded85fd1d515b5d0831
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012450B2

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