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Acetone → 1-(2-Chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylic acid hydrochloride

HRID 1732568
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반응식

HRID 1732568 반응식
Cl.[Cl:2][C:3]1[CH:19]=[CH:18][CH:17]=[CH:16][C:4]=1[CH2:5][N:6]1[CH2:11][CH2:10][CH:9]=[C:8]([C:12]([O:14]C)=[O:13])[CH2:7]1.CC(C)=O>Cl>[ClH:2].[Cl:2][C:3]1[CH:19]=[CH:18][CH:17]=[CH:16][C:4]=1[CH2:5][N:6]1[CH2:11][CH2:10][CH:9]=[C:8]([C:12]([OH:14])=[O:13])[CH2:7]1
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참가 물질

4

반응물 2

HCID 180AcetoneHCID 12769333Methyl 1-(2-chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride

생성물 1

HCID 127693701-(2-Chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylic acid hydrochloride수율 186.4%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A solution of methyl 1-(2-chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride (0.45 g.) in concentrated hydrochloric acid (10 ml.) was heated at 95°-100° C. for 2 hours, cooled and evaporated. The residue was evaporated several times with acetone and toluene to remove remaining traces of water. The solid obtained was stirred with acetone and then collected by filtration to give 1-(2-chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylic acid hydrochloride (0.4 g.), m.p. 208°-210° C. (dec.).

후처리

  1. temperaturecooled
  2. customevaporated
  3. customThe residue was evaporated several times with acetone and toluene
  4. customto remove
  5. customThe solid obtained
  6. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-59a7d37e3f3e47ed908a7c91e3692f74
출처 데이터셋
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04238488

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