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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylamine → 1,1-Dimethyl-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)urea

HRID 259321
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인쇄 미리보기

반응식

HRID 259321 반응식
[S:1]1[CH:5]=[CH:4][C:3]2[CH:6]([N:10]=[C:11]=[O:12])[CH2:7][CH2:8][CH2:9][C:2]1=2.[CH3:13][NH:14][CH3:15]>C(OCC)C>[CH3:13][N:14]([CH3:15])[C:11]([NH:10][CH:6]1[C:3]2[CH:4]=[CH:5][S:1][C:2]=2[CH2:9][CH2:8][CH2:7]1)=[O:12]
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참가 물질

4

반응물 2

HCID 674DimethylamineHCID 205373014-Isocyanato-4,5,6,7-tetrahydro-1-benzothiophene

생성물 1

HCID 203488931,1-Dimethyl-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)urea

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A solution of 6.27 grams of 4,5,6,7-tetrahydrobenzo[b]thien-4-yl isocyanate in 200 ml. of diethyl ether is charged with gaseous dimethylamine introduced via a capillary tube with stirring. After 0.5 hour of bubbling, the gas flow is terminated, and the mixture is evaporated to dryness to give a solid residue. This is crystallized from acetone-hexane-ether to give 1,1-dimethyl-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)urea melting at 117° C. to 120° C.

후처리

  1. additionintroduced via a capillary tube
  2. customAfter 0.5 hour of bubbling
  3. customthe gas flow is terminated
  4. customthe mixture is evaporated to dryness
  5. customto give a solid residue
  6. customThis is crystallized from acetone-hexane-ether

출처 및 근거

ORD 기록
ord-ced409063f364945a642ce72b14c391e
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04036979

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