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Sodium Hydroxide → HCID 12952797, 화합물

HRID 1995076
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HRID 1995076 반응식
Br.Br.[N:3]1([C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1.[N:16]([CH2:19][CH:20]([O:23][CH3:24])[O:21][CH3:22])=[C:17]=[S:18].[OH-].[Na+]>CO>[CH3:22][O:21][CH:20]([O:23][CH3:24])[CH2:19][NH:16][C:17]([N:6]1[CH2:5][CH2:4][N:3]([C:9]2[CH:10]=[CH:11][C:12]([OH:15])=[CH:13][CH:14]=2)[CH2:8][CH2:7]1)=[S:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 144710Isothiocyanatoacetaldehyde dimethyl acetalHCID 2723591p-(1-Piperazinyl)phenol dihydrobromide

생성물 1

HCID 12952797HCID 12952797, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 10.8 parts of 4-(1-piperazinyl)phenol dihydrobromide, 2.6 parts of 2-isothiocyanato-1,1-dimethoxyethane and 54 parts of methanol is stirred and refluxed for 30 minutes. Then there are added 4.7 parts of sodium hydroxide and the whole is stirred overnight at room temperature. The precipitated product is filtered off and crystallized from 4-methyl-2-pentanone, yielding 4.9 parts of N-(2,2-dimethoxyethyl)-4-(4-hydroxyphenyl)-1-piperazinecarbothioamide; mp. 161.4° C.

후처리

  1. temperaturerefluxed for 30 minutes
  2. stirringthe whole is stirred overnight at room temperature
  3. filtrationThe precipitated product is filtered off
  4. customcrystallized from 4-methyl-2-pentanone

출처 및 근거

ORD 기록
ord-21c65d1c551c453baec6fc3c3f3f3f43
출처 데이터셋
uspto-grants-1983_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04402957

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