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Methyl Methanesulfonate → HCID 19819114, 화합물

HRID 1195420
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인쇄 미리보기

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HRID 1195420 반응식
Cl[CH2:2][CH2:3][N:4]=[C:5]=[O:6].[CH3:7][S:8]([O:11]C)(=[O:10])=[O:9]>CS([O-])(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC>[N:4]([CH2:3][CH2:2][O:11][S:8]([CH3:7])(=[O:10])=[O:9])=[C:5]=[O:6]
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참가 물질

4

반응물 2

HCID 4156Methyl Methanesulfonate2회HCID 160352-Chloroethyl isocyanate2회

생성물 1

HCID 19819114HCID 19819114, 화합물

시약·촉매·용매 1

HCID 30176031-Butanaminium, N,N,N-tributyl-, methanesulfonate (1:1)촉매

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온도
120 °C

실험 절차

20.0 g (0.06 mol) of tetrabutylammonium methanesulfonate are added to a solution of 36.0 g (0.34 mol) of 2-chloroisocyanatoethane and 93.3 g (0.85 mol) of methyl methanesulfonate and the mixture is heated at 120° C for 6 hours. It is distilled in a thin layer evaporator at 180° C. under a pressure of 0.04 mbar and the crude product is purified by distillation. 18.0 g (0.17 mol) of 2chloroisocyanatoethane and 71.0 g (0.65 mol) of methyl methanesulfonate are recovered in this way.

후처리

  1. distillationIt is distilled in a thin layer evaporator at 180° C. under a pressure of 0.04 mbar
  2. distillationthe crude product is purified by distillation

출처 및 근거

ORD 기록
ord-d433e79b626e43a59a3c9c476aee80f4
출처 데이터셋
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05110975

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