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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972940Generated: October 31, 2026

Hydrochloric Acid → 1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid

https://huagongshe.com/reaction/1972940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant1-Boc-Azetidine-3-carboxylic acidHCID 2755981—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acidHCID 1098821460%

Reaction Steps

To a solution of 1-(tert-butoxycarbonyl)azetidine-3-carboxylic acid (3.00 g, 14.9 mmol) in MeOH (12.5 mL) was added 4M HCl in 1,4-dioxane (12.5 mL). The reaction was stirred at rt for 16 h. The mixture was evaporated to dryness. To a cooled (0° C.) solution of the residue in 1,4-dioxane (15 mL) and 2N aqueous NaOH (75 mL) was added benzyl chloroformate (2.67 g, 15.7 mmol), dropwise. The reaction was warmed to rt and was allowed to stir for 4 h. The mixture was washed with ethyl acetate (75 mL) and the aqueous layer was acidified (pH 5) with the addition of conc HCl. The mixture was extracted with ethyl acetate (3×75 mL) and the combined organic layers were washed with brine, dried (Na2SO4) and evaporated to give 2.10 g (60%) of the desired product. ES-MS m/z 235.90 [M+H]+, HPLC RT (min) 2.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-5b37111e75954858862dac0d8433d0d5
Source noteuspto-grants-2013_04