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

HRID 636772

反応式

HRID 636772 の反応式
[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]

参加物

3

反応物 2

HCID 123741,6-Hexanediol2 回HCID 3153171,4-Butanedisulfonyl dichloride

生成物 1

HCID 212557531,4-Butanedisulfonylchloride 1,6-hexanediol

実験手順

Next, the 1,6-hexanediol vapor in the condensing chamber 2 was adiabatically expanded, and the introduced base particles were exposed thereto for 15 minutes. Consequently, a polymerization reaction between 1,4-butanedisulfonyl chloride and 1,6-hexanediol took place on the surface of the base particles, forming a film of 1,4-butanedisulfonylchloride-1,6-hexanediol co-polymer.

出典と根拠

ORDレコード
ord-2c97b045242444c5ac9e42f873d8026d
出典データセット
uspto-grants-2001_02
特許番号
US06194487B1

関連ノート

読み込み中…