HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → n-Benzoyl-cis-4-hydroxy-d-proline methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl (2R,4R)-4-hydroxypyrrolidine-2-carboxylate hydrochloride | HCID 12764090 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-Benzoyl-cis-4-hydroxy-d-proline methyl ester | HCID 1476248 | 90.7% |
Reaction Steps
This ester was added in portions to a stirred mixture of 1500 mL of 1 N aqueous sodium bicarbonate and 500 mL of dichloromethane at 0-5° C., then 80 mL (97 g, 0.69 mol) of benzoyl chloride was added dropwise at 0-5° C., and the mixture was stirred at room temperature overnight. The phases were separated and the aqueous phase was extracted with dichloromethane (twice with 250 mL). The organic phases were combined, dried over magnesium sulfate, and evaporated under reduced pressure. The residue was triturated with toluene to afford 112.98 g (90.7% from cis4-hydroxy-D-proline) of N-benzoyl-cis-4-hydroxy-D-proline methyl ester as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664400B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-2292fd3a4d614286975d733427428fea |
| Source note | uspto-grants-2003_12 |