Methanol → (2R,4R)-methyl 4-hydroxypyrrolidine-2-carboxylate
Reaction equation
[OH:1][C@H:2]1[CH2:6][NH:5][C@@H:4]([C:7]([OH:9])=[O:8])[CH2:3]1.[CH3:10]O>>[CH3:10][O:8][C:7]([C@H:4]1[CH2:3][C@@H:2]([OH:1])[CH2:6][NH:5]1)=[O:9]Participants
3
Conditions
- Temperature
- 0 °C
Procedure
Cis-4-Hydroxy-D-proline (15 g, 115 mmol) was suspended in 150 mL anhydrous methanol under an argon atmosphere, then cooled to 0° C. before bubbling in HCl gas for 15 minutes. The solution gradually became homogenous. The argon and HCl gas lines were removed and the solution was refluxed for 4 h. The solution was cooled and then concentrated under reduced pressure. The crude material was redissolved in 100 mL methanol and diethyl ether was added until a precipitate formed. The precipitate was filtered off, washed with diethyl ether, and dried in vacuo overnight to reveal 1 (20 g, 95%) as a white solid. MS: APCI (AP+): 146 (M)+.
Workup
- custombefore bubbling in HCl gas for 15 minutes
- customThe argon and HCl gas lines were removed
- temperaturethe solution was refluxed for 4 h
- temperatureThe solution was cooled
- concentrationconcentrated under reduced pressure
- dissolutionThe crude material was redissolved in 100 mL methanol
- additiondiethyl ether was added until a precipitate
- customformed
- filtrationThe precipitate was filtered off
- washwashed with diethyl ether
- customdried in vacuo overnight
Sources & evidence
- ORD record
- ord-f48c433ec2214e50bbcbe41669a536b3
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07030141B2
Reaction notes
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