HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → methyl 4-[(2S,4S)-1-tert-butoxycarbonyl-4-hydroxy-2-pyrrolidinyl]methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | methyl 4-[(2S,4S)-4-acetoxy-1-tert-butoxycarbonyl-4-hydroxy-2-pyrrolidinyl]methoxybenzoate | HCID 69334609 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl 4-[(2S,4S)-1-tert-butoxycarbonyl-4-hydroxy-2-pyrrolidinyl]methoxybenzoate | HCID 16093638 | 87% |
Reaction Steps
To a stirred solution of methyl 4-[(2S,4S)-4-acetoxy-1-tert-butoxycarbonyl-4-hydroxy-2-pyrrolidinyl]methoxybenzoate (7.43 g, 18.9 mmol) in MeOH (150 ml) was added cat. K2CO3 at room temperature. After 1 day stirring, the mixture was concentrated in vacuo. The resulting residue was recrystallized by the addition of CHCl3-n-hexane, to give methyl 4-[(2S,4S)-1-tert-butoxycarbonyl-4-hydroxy-2-pyrrolidinyl]methoxybenzoate (5.76 g, 87%) as a colorless solid. 1H-NMR (CDCl3) δ1.46 (s, 9H), 2.11 (m, 1H), 2.35 (br, 1H), 3.27-3.65 (m, 2H), 3.89 (s, 3H), 4.07-4.54 (m, 4H), 6.96 (d, J=6.9 Hz, 2H), 7.99 (d, J=6.9 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06756378B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-59741f75b5124df292a95fc10fe10ecb |
| Source note | uspto-grants-2004_06 |