Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722480Generated: October 26, 2026

Water → 1-benzylazetidine-3,3-dicarboxylic Acid

https://huagongshe.com/reaction/1722480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
Reactant[1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanolHCID 20164320—
CatalystNickel SulfateHCID 24586—
Product1-benzylazetidine-3,3-dicarboxylic AcidHCID 11310885—

Reaction Steps

Bromine (10.6 g) was slowly added at 20° C. over 8 hours to a mixture of N-benzyl-3,3-bis(hydroxymethyl)azetidine (2.1 g) in water (50 ml) containing sodium hydroxide (9.3 g) and nickel chloride 6.0 aq. (1.5 g). After stirring overnight, the green precipitate of nickel hydroxide was filtered off, and the filtrate evaporated to dryness. The residue was boiled in ethanol, and the insoluble material (desired product as sodium salt and sodium bromide) separated and worked up to yield the N-benzyl-azetidine-3,3-dicarboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855452
Source datasetuspto-grants-1989_08
ORD IDord-2c659e65c5bc4e558fb6affc643a49c5
Source noteuspto-grants-1989_08