HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 2-amino-3-(4-nitrophenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Nitro-3-phenyl-L-alanine | HCID 13706 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | Methyl 2-amino-3-(4-nitrophenyl)propanoate | HCID 560520 | — |
Reaction Steps
To a suspension of 4-nitrophenylalanine 1 (25 g) in methanol (10 ml/g) at 0° C. is added SOCl2 (2 equ.). After 30 minutes, the reaction is stirred at room temperature for 1 night. Volatiles are then evaporated and the residue is diluted in water. The solution is alkalinized with NaOH 2N and extracted with CH2Cl2. The organic phase is dried over MgSO4 and evaporated. No further purification is needed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07638630B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-6073044826314e0293aa2d3dd5eab324 |
| Source note | uspto-grants-2009_12 |