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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390081Generated: November 3, 2026

Acetic Acid → HCID 70573560, compound

https://huagongshe.com/reaction/1390081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70574273HCID 70574273—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 70573560HCID 70573560—

Reaction Steps

A solution of (3-amino-4-phenoxy-5-sulfamylbenzyl)allylamine hydrate (3.3 g; prepared as described in Example 111) and benzaldehyde (1.2 g) in methanol (35 ml) is refluxed for 16 hours. Sodium borohydride (1.0 g) is then during 30 minutes added in portions while stirring at 0°-5° C. After additional stirring for 2 hours, acetic acid (1.0 ml) followed by water (120 ml) is cautiously added to precipitate crude (3-benzylamino-4-phenoxy-5-sulfamylbenzyl)allylamine. After filtration and recrystallization twice from aqueous ethanol, it is obtained with a melting point of 139°-140° C. The material (IR, analysis) is identical with the material prepared as in Example 150.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04247550
Source datasetuspto-grants-1981_01
ORD IDord-af311fcdb4b44e259d8a2772de1cafb5
Source noteuspto-grants-1981_01