HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl alpha-amino-p-methoxycarbonylmethylphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Methyl alpha-tert-butoxycarbonylamino-p-methoxycarbonylmethyl-phenylacetate | HCID 54316225 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diethyl ether methanol | HCID 21864698 | — |
| Product | Methyl alpha-amino-p-methoxycarbonylmethylphenylacetate | HCID 54294376 | — |
Reaction Steps
To a solution of methyl α-tert-butoxycarbonylamino-p-methoxycarbonylmethyl-phenylacetate (2.86 g, 8.5 mmol) in CH2Cl2 (10 ml) cooled at 0° C. was added 10 ml of TFA. After stirring for 1 hour at room temperature the reaction mixture was evaporated to dryness. The resulting solid was dissolved in ethyl acetate and water and the pH was adjusted to 8 with NaHCO3. After extraction with ethyl acetate the organic layers were washed with brine, dried and evaporated to give a yellow oil. After dissolution of this oil in a mixture of ether:methanol (10:1 v/v) a saturated solution of HCl in ether was added to give, after filtration, methyl α-amino-p-methoxycarbonyl-methylphenylacetate (2.2 g, 96%) as a white solid, m.p. 189.2°-189.6° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05747499 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-9ec8b2b771ad4249893cd9784f39e532 |
| Source note | uspto-grants-1998_05 |