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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098415Generated: October 30, 2026

4-Methylbenzylamine → 2,2-difluoro-N-(4-methylbenzyl)ethanamine

https://huagongshe.com/reaction/2098415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylbenzylamineHCID 66035—
ReactantChlorodifluoroethane (mixed isomers)HCID 2736499—
SolventWaterHCID 962—
Product2,2-difluoro-N-(4-methylbenzyl)ethanamineHCID 6092306858%

Reaction Steps

An amount of 26.2 g (242 mmol) of 2,2-difluoro-1-chloroethane and 10 g of 4-methylbenzylamine (80.8 mmol) are heated in an autoclave at an internal temperature of 120° C. for 16 hours. Subsequently, 50 g of water are added and the aqueous phase is separated. The aqueous phase is again extracted with 2,2-difluoro-1-chloroethane and the combined organic phases are distilled as described in Example 1.1. Here also, the 4-methylbenzylamine hydrochloride which is present in the aqueous phase can be converted back into free 4-methylbenzylamine by addition of sodium hydroxide solution. After distillation, 4.3 g of 2,2-difluoro-N-(4-methylbenzyl)ethanamine are obtained, which corresponds to a yield of 58%, based on reacted 4-methylbenzylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450528B2
Source datasetuspto-grants-2013_05
ORD IDord-a9015e25fd45480f8288826f21702d51
Source noteuspto-grants-2013_05