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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579711Generated: November 4, 2026

Hydrogen Bromide → 4-[(2-Methylhydrazino)-methyl]-benzoic acid [2-hydroxy-3,3,3-trichloropropyl]amide hydrobromide

https://huagongshe.com/reaction/1579711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantDichloromethaneHCID 6344—
ReactantPropanol, 3-amino-1-trichloro-HCID 215437—
Reactant4-[(2-Methyl-1,2-dicarbobenzoxy-hydrazino)-methyl]-benzoyl chlorideHCID 21569059—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-[(2-Methylhydrazino)-methyl]-benzoic acid [2-hydroxy-3,3,3-trichloropropyl]amide hydrobromideHCID 131709890—

Reaction Steps

15.8 g. of 4-[(2-methyl-1,2-dicarbobenzoxy-hydrazino)methyl]-benzoyl chloride were dissolved in 50 ml. of methylene chloride. This solution was added, while stirring, dropwise to a suspension of 12.6 g. of 2-hydroxy-3,3,3-trichloro-propylamine in 150 ml. of methylene chloride. Stirring was continued for 2 hours at room temperature and 30 minutes at 40°, whereupon 50 ml. of water were added thereto. The product was worked up according to Example 3 and treated with hydrogen bromide in glacial acetic acid. The crystalline crude material was recrystallized from ethanol/acetonitrile/ether, yielding 4-[(2-methylhydrazino)-methyl]-benzoic acid [2-hydroxy-3,3,3-trichloropropyl]amide hydrobromide melting at 187°-189° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931268
Source datasetuspto-grants-1976_01
ORD IDord-ad9b02f778a642cdb976f29f13b2393d
Source noteuspto-grants-1976_01