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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994426Generated: October 30, 2026

Sodium Hydroxide → Ethanamine, N-(2,2-diethoxyethyl)-2,2-difluoro-

https://huagongshe.com/reaction/1994426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,2-DiethoxyethylamineHCID 69524—
Reactant1-Ethoxy-2,2-difluoroethanolHCID 2758246—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventDichloromethane methanolHCID 21226129—
ProductEthanamine, N-(2,2-diethoxyethyl)-2,2-difluoro-HCID 7900682369.9%

Reaction Steps

A solution of 3 g (22.5 mmol) of 1-amino-2,2-diethoxyethane, 3.1 g (24.8 mmol) of difluoroacetaldehyde ethyl hemiacetal and 1 pellet of solid NaOH in 44 ml of toluene was heated at 120° C. with a Dean-Stark trap for 1.5 hours. The mixture was left to stand until it had cooled to room temperature and was concentrated in vacuo. The residue was diluted with 80 ml of methanol, and 3.4 g (90 mmol) of sodium borohydride were added in small quantities. The reaction mixture was then stirred overnight, concentrated in vacuo and partitioned between ethyl acetate and water. The organic phase was isolated, dried (MgSO4) and concentrated in vacuo. 3.7 g of crude substance were obtained as a colorless oil. The residue was subjected to a flash chromatography on 40 g of SiO2 (elution with DCM/MeOH, gradient 1-8%). 3.1 g of the desired amine were obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652007B2
Source datasetuspto-grants-2010_01
ORD IDord-03fa7bb94d22434db32c2506de69ed47
Source noteuspto-grants-2010_01