Methanol → Methyl 4-nitro-L-phenylalaninate hydrochloride
Reaction equation
S(Cl)([Cl:3])=O.[N+:5]([C:8]1[CH:19]=[CH:18][C:11]([CH2:12][C@@H:13]([C:15]([OH:17])=[O:16])[NH2:14])=[CH:10][CH:9]=1)([O-:7])=[O:6].[CH3:20]O>>[ClH:3].[CH3:20][O:16][C:15](=[O:17])[C@H:13]([CH2:12][C:11]1[CH:10]=[CH:9][C:8]([N+:5]([O-:7])=[O:6])=[CH:19][CH:18]=1)[NH2:14]Participants
4
Procedure
Thionyl chloride (distilled, 0.69 ml, 9.5 mmol) was added dropwise to methanol (20 ml) at 31 10° C. p-Nitro-L-phenylalanine (1.00 g, 4.76 mmol) was added and the solution stirred 24 hours at room temperature. After evaporating to dryness, the residue was recrystallized from methanol/ether to give 1.00 g of a white solid melting at 218°-219° C. [α]25 =+11.5° (c=0.9, H2O).
Workup
- additionwas added
- customAfter evaporating to dryness
- customthe residue was recrystallized from methanol/ether
Sources & evidence
- ORD record
- ord-16d7da687c2e4ff183591bf738886a2c
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04837305
Reaction notes
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