Trifluoroacetic acid → HCID 40531003, compound

HRID 1864837Notes

Reaction equation

HRID 1864837 reaction equation
[CH3:1][C@@H:2]1[O:7][CH2:6][C@@H:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:4](C(OC(C)(C)C)=O)[C:3]1=[O:21].C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH3:1][C@@H:2]1[O:7][CH2:6][C@@H:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[NH:4][C:3]1=[O:21]

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 66972967HCID 66972967, compound

Product 1

HCID 40531003HCID 40531003, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of tert-butyl (2S,5R)-2-methyl-3-oxo-5-phenylmorpholine-4-carboxylate from Step D (160 mg, 0.55 mmol) in CH2Cl2 (2 mL) at ambient temperature was added TFA (0.41 mL, 5.5 mmol). After stirring for 1 h, the reaction mixture was concentrated in vacuo to give the title compound. MS: m/z=192 (M+1).

Workup

  1. concentrationthe reaction mixture was concentrated in vacuo

Sources & evidence

ORD record
ord-140482ec1da84158a40b2cffae5de27a
Source dataset
uspto-grants-2009_12
Patent number
US07625901B2

Reaction notes

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