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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Reactant | 1-Ethoxy-2,2-difluoroethanol | HCID 2758246 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | Ethanamine, N-(2,2-diethoxyethyl)-2,2-difluoro- | HCID 79006823 | 69.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07652007B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-03fa7bb94d22434db32c2506de69ed47 |
|---|
| Source note | uspto-grants-2010_01 |
|---|