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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide → Cyclopropanecarboxylic Acid 4-chloro-3-formyl-benzylamide

HRID 2428136
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HRID 2428136 반응식
[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][NH:7][C:8]([CH:10]2[CH2:12][CH2:11]2)=[O:9])=[CH:4][C:3]=1[CH2:15][OH:16]>CC#N.O=[Mn]=O>[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][NH:7][C:8]([CH:10]2[CH2:11][CH2:12]2)=[O:9])=[CH:4][C:3]=1[CH:15]=[O:16]
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참가 물질

4

반응물 1

HCID 67148310Cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide

생성물 1

HCID 86632362Cyclopropanecarboxylic Acid 4-chloro-3-formyl-benzylamide수율 94.1%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매3회HCID 6342Acetonitrile용매

실험 절차

MnO2 (6.29 g, 72.0 mmol) was added to a sol. of cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide (3.47 g, 14.0 mmol) in CH3CN (300 mL) at rt. The mixture was stirred for 3 h at rt, and MnO2 (2.52 g, 29.0 mmol) was added again. The mixture was stirred for 1 h at rt, and MnO2 (1.26 g, 14.0 mmol) was added again. The mixture was stirred for 1.5 h, and was filtered through celite. The filtrate was evaporated under reduced pressure, and the residue was dried under high vacuum to yield the crude title compound (3.13 g, 91%) that was used further without purification. LC-MS: tR=0.80 min; ES+: 279.31.

후처리

  1. stirringThe mixture was stirred for 1 h at rt
  2. stirringThe mixture was stirred for 1.5 h
  3. filtrationwas filtered through celite
  4. customThe filtrate was evaporated under reduced pressure
  5. customthe residue was dried under high vacuum

출처 및 근거

ORD 기록
ord-e40a95dcfb6343469488598a3c7562c6
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968720B2

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