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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → 6-(Hydroxymethyl)pyridine-2-carbonitrile

HRID 1246666
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HRID 1246666 반응식
[C:1]([C:3]1[CH:11]=[CH:10][C:6](C(O)=O)=[CH:5][N:4]=1)#[N:2].CCN(CC)CC.Cl[C:20](OCC)=[O:21].[BH4-].[Na+]>C1COCC1>[OH:21][CH2:20][C:5]1[N:4]=[C:3]([C:1]#[N:2])[CH:11]=[CH:10][CH:6]=1
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 10928Ethyl chloroformateHCID 27611086-Cyanopyridine-3-carboxylic acidHCID 4311764Sodium borohydride

생성물 1

HCID 147614586-(Hydroxymethyl)pyridine-2-carbonitrile수율 36.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 6-cyanonicotinic acid (12 g, 0.081 mol; see step (i) above) in THF at 0° C., Et3N (12.4 mL, 0.0892 mol) was added followed by ethyl chloroformate (8.53 mL, 0.0892 mol). The reaction mixture was stirred for 15 min and NaBH4 (6.14 g, 0.162 mol) was added. Then the mixture was stirred at RT overnight, quenched with water and extracted with methylene chloride. The organic layer was concentrated and purified by column chromatography to yield 4 g (20%) of the alcohol.

후처리

  1. stirringThen the mixture was stirred at RT overnight
  2. customquenched with water
  3. extractionextracted with methylene chloride
  4. concentrationThe organic layer was concentrated
  5. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-0241f58821ee42dc91fe93b06ca869c6
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07129233B2

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