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Hydrochloric Acid → N-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amine hydrochloride

HRID 882334
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HRID 882334 반응식
[ClH:1].[F:2][C:3]1[CH:19]=[CH:18][C:6]([CH2:7][NH:8][C@@H:9]2[CH2:11][C@H:10]2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:5][CH:4]=1>CCOCC>[ClH:1].[F:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][NH:8][C@@H:9]2[CH2:11][C@H:10]2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:18][CH:19]=1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 46869734N-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amine

생성물 1

HCID 66629772N-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amine hydrochloride수율 83.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
-78 °C

실험 절차

2 M ethereal solution of HCl (0.24 mL, 0.47 mmol) was slowly added to a solution of N-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amine (95 mg, 0.39 mmol) in dry Et2O (10 mL) cooled at −78° C., and allowed to reach room temperature. After 10 min the white precipitate was allowed to settle and Et2O was decanted, the solid was washed with Et2O (10 mL) and vacuum dried, rendering 90 mg of N-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amine hydrochloride (white solid, 83% yield).

후처리

  1. customto reach room temperature
  2. customEt2O was decanted
  3. washthe solid was washed with Et2O (10 mL) and vacuum
  4. customdried

출처 및 근거

ORD 기록
ord-b0bbc109f1064c8ebe29c3111d58e128
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993808B2

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