Methanol → HCID 66764016, compound
Reaction equation
[NH2:1][CH:2]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-:16])=[O:15])[CH:9]=1)[CH2:3][CH2:4][C:5]([OH:7])=[O:6].S(Cl)(Cl)=O.[CH3:21]O>>[CH3:21][O:6][C:5](=[O:7])[CH2:4][CH2:3][CH:2]([NH2:1])[C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-:16])=[O:15])[CH:9]=1Participants
4
Procedure
680 mg (2.49 mmol) 4-Amino-4-(3-nitro-phenyl)-butyric acid were suspended in 5 ml methanol and 635 μl (8.75 mmol) thionyl chloride were added. The mixture was stirred at room temperature overnight. The reaction mixture was evaporated to dryness, methanol was added and again evaporated to dryness.
Workup
- customThe reaction mixture was evaporated to dryness, methanol
- additionwas added
- customagain evaporated to dryness
Sources & evidence
- ORD record
- ord-57935829f1f74a9abdc61db098206a6f
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040560B2
Reaction notes
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