HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082872Generated: October 30, 2026
Diethyl Ether → 3-Amino-2-benzyl-5-(hydroxymethyl)benzene-1-sulfonamide
https://huagongshe.com/reaction/2082872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methyl 3-amino-4-benzyl-5-sulfamoylbenzoate | HCID 20294631 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-Amino-2-benzyl-5-(hydroxymethyl)benzene-1-sulfonamide | HCID 53686929 | — |
Reaction Steps
To a stirred mixture of lithium aluminium hydride (12 g) and dry diethyl ether (350 ml), a solution of methyl 3-amino-4-benzyl-5-sulfamylbenzoate (30 g) in dry pyridine (300 ml) is dropwise added during 1-1.5 hours. After additional stirring for 3 hours, the mixture is cooled and ethyl acetate (25 ml) followed by water (50 ml) are very cautiously added dropwise. After stirring for a further 30 minutes, the solids are collected by filtration and dried in air. The filter cake is treated with hot 4 N hydrochloric acid (about 500 ml) to dissolve inorganic material. After cooling 3-amino-4-benzyl-5-sulfamylbenzyl alcohol is collected by filtration and dried in air. After recrystallization from aqueous ethanol it is obtained with a melting point of 159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04082851 |
|---|
| Source dataset | uspto-grants-1978_04 |
|---|
| ORD ID | ord-baea04da22db4f8cabc7e85726a31d2a |
|---|
| Source note | uspto-grants-1978_04 |
|---|