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Trichloroacetyl chloride → N-[(1S)-2-Hydroxy-1,2-dimethylpropyl]-2,2,2-trichloroethanamide

HRID 2392823
Notes
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Reaction equation

HRID 2392823 reaction equation
[NH2:1][C@@H:2]([CH3:7])[C:3]([CH3:6])([OH:5])[CH3:4].[Cl:8][C:9]([Cl:14])([Cl:13])[C:10](Cl)=[O:11]>N1C=CC=CC=1>[OH:5][C:3]([CH3:6])([CH3:4])[C@@H:2]([NH:1][C:10](=[O:11])[C:9]([Cl:14])([Cl:13])[Cl:8])[CH3:7]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6420Trichloroacetyl chlorideHCID 51415372(S)-3-Amino-2-methylbutan-2-OL

Product 1

HCID 86753059N-[(1S)-2-Hydroxy-1,2-dimethylpropyl]-2,2,2-trichloroethanamideYield 94%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

To a solution of (3) (1.193 g, 8.56 mmol) at 0° C. in pyridine (24 ml) was added trichloroacetyl chloride (1.05 ml, 9.41 mmol). After stirring at this temperature for 10 minutes, the reaction mixture was stirred overnight at room temperature. The reaction was quenched by the addition of saturated aqueous sodium chloride solution, after which the product was extracted with dichloromethane and the combined organic extracts were washed with hydrochloric acid (1M). Concentration in vacuo and purification by flash column chromatography using 30% ethyl acetate/40-60 petroleum ether as eluant furnished the title compound (4) (1.992 g, 94%) as an oil; νmax (CH2Cl2) 1713 cm-1 ; [α]D24 (c 1.2 in CHCl3)=+6.3; (Found: C, 33.71; H, 5.12; N, 5.72. C7H12Cl3NO2 requires C, 33.83; H, 4.87; N, 5.64%); δH (200 MHz; CDCl3) 1.21 (3H, d, J=3.4, CH3CH), 1.25 (3H, s, C(CH3)2), 1.26 (3H, s, C(CH3)2), 2.31 (1H, s, OH), 3.82 (1H, dq, J=6.7 and 8.8, CHCH3NH), 7.1 (1H, s, NH); δC (125 MHz; CDCl3) 14.89 (CH3), 26.68 (CH3), 27.56 (CH3), 55.19 (CH), 72.01 (C), 92.82 (CCl3), 161.56 (CO); m/z (CI+, NH3) 248 (M+).

Workup

  1. stirringthe reaction mixture was stirred overnight at room temperature
  2. customThe reaction was quenched by the addition of saturated aqueous sodium chloride solution
  3. extractionafter which the product was extracted with dichloromethane
  4. washthe combined organic extracts were washed with hydrochloric acid (1M)
  5. concentrationConcentration
  6. customin vacuo and purification by flash column chromatography

Sources & evidence

ORD record
ord-0aae67103a7a4589af3838a01239e3ba
Source dataset
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05801249

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes