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N,N-Dimethylthioformamide → 4-(Diphenylmethyl)-1-piperidinecarbothioaldehyde

HRID 1413949
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인쇄 미리보기

반응식

HRID 1413949 반응식
[C:1]1([CH:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CN(C)[CH:22]=[S:23]>C1(C)C=CC=CC=1>[C:1]1([CH:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:8]2[CH2:9][CH2:10][N:11]([CH:22]=[S:23])[CH2:12][CH2:13]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 69794N,N-DimethylthioformamideHCID 882784-Benzhydrylpiperidine

생성물 1

HCID 130978784-(Diphenylmethyl)-1-piperidinecarbothioaldehyde

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of 20.0 g (0.08 mole) of 4-diphenylmethylpiperidine, 14.2 g (0.16 mole) of N,N-dimethylthioformamide and 50 ml of toluene was refluxed for 12 hours, cooled, and washed with water. The organic layer was separated, dried and stripped to an oil which was treated with diethyl ether to give a solid. Recrystallization of this material afforded a white crystalline solid, 4-(diphenylmethyl)-1-piperidinecarbothioaldehyde, m.p. 152°-154° C.

후처리

  1. temperaturecooled
  2. washwashed with water
  3. customThe organic layer was separated
  4. customdried
  5. additionwas treated with diethyl ether
  6. customto give a solid
  7. customRecrystallization of this material

출처 및 근거

ORD 기록
ord-b44088f2149a48bdb88cede096132365
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04251655

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