1,6-Hexanediol → 1,4-Butanedisulfonylchloride 1,6-hexanediol

HRID 636774

반응식

HRID 636774 반응식
[CH2:1]([OH:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][OH:7].[CH2:9]([S:17]([Cl:20])(=[O:19])=[O:18])[CH2:10][CH2:11][CH2:12][S:13]([Cl:16])(=[O:15])=[O:14]>>[CH2:9]([S:17]([Cl:20])(=[O:18])=[O:19])[CH2:10][CH2:11][CH2:12][S:13]([Cl:16])(=[O:15])=[O:14].[CH2:1]([OH:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][OH:7]

참가 물질

3

반응물 2

HCID 123741,6-Hexanediol2회HCID 3153171,4-Butanedisulfonyl dichloride

생성물 1

HCID 212557531,4-Butanedisulfonylchloride 1,6-hexanediol

실험 절차

Next, the 1,6-hexanediol vapor in the condensing chamber 2 was adiabatically expanded, and the introduced modified particles (17) were exposed thereto for 18 minutes. Consequently, a further polymerization reaction between 1,4-butanedisulfonyl chloride and 1,6-hexanediol took place on the surface of the modified particles (17), forming a film of 1,4-butanedisulfonylchloride-1,6-hexanediol co-polymer.

출처 및 근거

ORD 기록
ord-c5d564ad008347688692e1eb2786a44f
출처 데이터셋
uspto-grants-2001_02
특허 번호
US06194487B1

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