4-Toluenesulfonyl chloride → HCID 22495477, compound

HRID 1935373Notes

Reaction equation

HRID 1935373 reaction equation
[C:1]([N:20]([CH2:24][CH2:25][OH:26])[CH2:21][CH2:22][OH:23])([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:27]1([CH3:37])[CH:32]=[CH:31][C:30]([S:33](Cl)(=[O:35])=[O:34])=[CH:29][CH:28]=1>>[C:1]([N:20]([CH2:24][CH2:25][O:26][S:33]([C:30]1[CH:31]=[CH:32][C:27]([CH3:37])=[CH:28][CH:29]=1)(=[O:35])=[O:34])[CH2:21][CH2:22][O:23][S:33]([C:30]1[CH:31]=[CH:32][C:27]([CH3:37])=[CH:28][CH:29]=1)(=[O:35])=[O:34])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 73974-Toluenesulfonyl chlorideHCID 4435488Ethanol, 2,2'-[(triphenylmethyl)imino]bis-

Product 1

HCID 22495477HCID 22495477, compound

Procedure

From N-trityldiethanolamine and p-toluenesulfonyl chloride.

Sources & evidence

ORD record
ord-cc9ada858c8a4a81b9e6daa395d72f78
Source dataset
uspto-grants-2002_05
Patent number
US06387891B2

Reaction notes

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