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

HRID 1994426Notes

Reaction equation

HRID 1994426 reaction equation
[NH2:1][CH2:2][CH:3]([O:7][CH2:8][CH3:9])[O:4][CH2:5][CH3:6].C(O[CH:13](O)[CH:14]([F:16])[F:15])C.[OH-].[Na+].[BH4-].[Na+]>C1(C)C=CC=CC=1.CO.CO.C(Cl)Cl>[CH2:5]([O:4][CH:3]([O:7][CH2:8][CH3:9])[CH2:2][NH:1][CH2:13][CH:14]([F:16])[F:15])[CH3:6]

Participants

8

Procedure

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.

Workup

  1. waitThe mixture was left
  2. concentrationwas concentrated in vacuo
  3. additionwere added in small quantities
  4. concentrationconcentrated in vacuo
  5. custompartitioned between ethyl acetate and water
  6. customThe organic phase was isolated
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo
  9. custom3.7 g of crude substance were obtained as a colorless oil

Sources & evidence

ORD record
ord-03fa7bb94d22434db32c2506de69ed47
Source dataset
uspto-grants-2010_01
Patent number
US07652007B2

Reaction notes

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