4-Toluenesulfonyl chloride → 1,6-Diisocyanohexane

반응식

[CH:1]([NH:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][NH:10][CH:11]=O)=O.C1(C)C=CC(S(Cl)(=O)=O)=CC=1>>[N+:3]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][N+:10]#[C-:11])#[C-:1]

참가 물질

반응물 2

HCID 73974-Toluenesulfonyl chloride

HCID 252508N-(6-formamidohexyl)formamide

생성물 1

HCID 33911051,6-Diisocyanohexane

실험 절차

1,6-diisocyanohexane was prepared by dehydration of N,N'-diformyl-(1,6-diaminohexane) with p-toluene sulfonyl chloride, essentially as described by Heztler and Covey (N. R. Heztler and E. J. Corey (1918), J. Org. Chem. 23 1222).

출처 및 근거

ORD 기록: ord-ee13330ab1e84a6f8b8dcbd6ea9fb9f6
출처 데이터셋: uspto-grants-1976_07
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US03970597

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