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Lead carbonate (PbCO3) → N-n-octyl-N'-(2-phenyl-2-propyl)carbodiimide

HRID 1438808
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HRID 1438808 반응식
[CH2:1]([NH:9][C:10]([NH:12][C:13]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)([CH3:15])[CH3:14])=S)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C(=O)([O-])[O-].[Pb+2]>C1(C)C(C)=CC=CC=1>[CH2:1]([N:9]=[C:10]=[N:12][C:13]([C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1)([CH3:14])[CH3:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
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참가 물질

4

반응물 2

HCID 11727Lead carbonate (PbCO3)HCID 13065174N-Octyl-N'-(2-phenylpropan-2-yl)thiourea

생성물 1

HCID 53849568N-n-octyl-N'-(2-phenyl-2-propyl)carbodiimide수율 80%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

A mixture of 14.2 grams of N-n-octyl-N'-(2-phenyl-2-propyl)-thiourea, 20 grams of basic lead carbonate and 100 ml of dry xylene was heated under reflux for 3 hours. The reaction liquid was then separated by filtration followed by concentration of the mother liquor, whereupon N-n-octyl-N'-(2-phenyl-2-propyl)carbodiimide of high purity was obtained. When this was distilled further, 10.1 grams of the intended product of b.p. 121°-3° C./0.15 mmHg was obtained as a pure product.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 3 hours
  3. customThe reaction liquid
  4. customwas then separated by filtration
  5. customwas obtained
  6. distillationWhen this was distilled further

출처 및 근거

ORD 기록
ord-4b8c13b6fa2c4896950dadd22cdc7fdd
출처 데이터셋
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04056631

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