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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065654Generated: October 25, 2026

Hydrochloric Acid → (2S)-1-((benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acid

https://huagongshe.com/reaction/1065654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
ReactantL-Proline, 4-hydroxy-, cis-HCID 69248—
ReactantPotassium BicarbonateHCID 516893—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(2S)-1-((benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 12731799—

Reaction Steps

26.5 g. (0.02 mole) of 4-hydroxy-L-proline and 32.8 ml. (0.23 mole) of benzyl chloroformate are reacted in 200 ml. of water and 100 ml. of acetone in the presence of 20 g. (0.02 mole) of potassium bicarbonate and 69.2 g. (0.50 mole) of potassium carbonate and worked up with 90 ml. of concentrated hydrochloric acid as described in Can.J. Biochem. & Physiol. 37, 584 (1959) to obtain N-carbobenzyloxy-4-hydroxy-L-proline. This product is reacted with cyclohexylamine to form the cyclohexylamine salt yield 69 g., m.p. 193°-195°. The salt (34 g.) is neutralized with N-hydrochloric acid to obtain 27 g. of free acid as a colorless glass [α]D26 -70°, (c, 1% in chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04330548
Source datasetuspto-grants-1982_05
ORD IDord-0f9b8529a9d845afab6d953ea54f3e22
Source noteuspto-grants-1982_05