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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245684Generated: October 30, 2026

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

https://huagongshe.com/reaction/245684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl succinimido carbonateHCID 83172—
Reactant3-azetidinecarboxylic AcidHCID 93192—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acidHCID 1098821488.2%

Reaction Steps

To azetidine-3-carboxylic acid (49.5 mmol, 5 g) in dioxane (150 ml), water (150 ml) and triethylamine (54.4 mmol, 7.58 ml) was added N-(benzyloxycarbonyloxy)succinimide (51.9 mmol, 12.94 g) and stirred at room temperature for half an hour. The reaction mixture was quenched with water and 30 ml of 2N hydrochloric acid and extracted three times with dichloromethane. The organic layers were combined, filtered through a phase separation filter and concentrated in vacuo. The residue was dissolved in dichloromethane and extracted three times with aqueous saturated sodium hydrogencarbonate solution. The aqueous layers were combined, acidified with 2N hydrochloric acid and extracted three times with dichloromethane. The organic layers were combined, washed with brine, filtered through a phase separation filter and concentrated in vacuo to give 1-(benzyloxycarbonyl)azetidine-3-carboxylic acid (10.27 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658794B2
Source datasetuspto-grants-2014_02
ORD IDord-53da7230223e42cdb15b9b467e6d8965
Source noteuspto-grants-2014_02