Ethanolamine → 4-Fluoro-N-(2-hydroxyethyl)benzenesulfonamide

HRID 351687Notes

Reaction equation

HRID 351687 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH2:12]([CH2:14][NH2:15])[OH:13]>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:15][CH2:14][CH2:12][OH:13])(=[O:10])=[O:9])=[CH:4][CH:3]=1

Participants

3

Procedure

The title compound was prepared according to the procedure of Intermediate 33 from 3.97-g (20 mmol) of 4-fluorobenzenesulfonyl chloride and 3.11 g (50 mmol) of ethanolamine, yielding 3.0 g of a white solid; m.p. 77-78° C.; MS (ES) m/z 219.8 (MH+); HRMS (EI) Calcd. for C8H10FNO3S (M+): 219.0366, Found: 219.0369.

Sources & evidence

ORD record
ord-6503ae986b254cc1aedbc92bf5e850ad
Source dataset
uspto-grants-2004_06
Patent number
US06743787B2

Reaction notes

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