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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264470Generated: November 2, 2026

Hydrochloric Acid → (2S)-1-(1,2-Dioxo-3,3-dimethylpentyl)azetidine-2-carboxylic acid

https://huagongshe.com/reaction/1264470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantLithium HydroxideHCID 3939—
Reactant(2S)-Methyl-1-(1,2-dioxo-3,3-dimethylpentyl)-azetidine-2-carboxylateHCID 59049321—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(2S)-1-(1,2-Dioxo-3,3-dimethylpentyl)azetidine-2-carboxylic acidHCID 5904930467%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2S)-Methyl-1-(1,2-dioxo-3,3-dimethylpentyl)-azetidine-2-carboxylate from Reference Example 3 (0.64 g, 2.65 mmol) in a 1:1 mixture of ether:methanol (20.0 mL) was added LiOH in water (4.9 mL, 1N solution) at about 0° C. The mixture was stirred at about 0° C. for about 30 minutes and then at about room temperature overnight. The pH was adjusted to about pH 1 by adding 1N HCl, then the mixture was diluted with water and extracted with dichloromethane. The organic layers were washed with brine and dried over sodium sulfate and then concentrated to give 0.40 g (67% yield) of the product as a yellow semisolid. 1H NMR (DMSO) δ 0.77-0.83 (m, 3H); 1.20-1.29 (series of s, 6H); 1.49-2.84 (series of m, 4H); 4.02-4.43 (series of m, 2H); 5.01-5.31 (series of dd, 1H); 6.10-6.80 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544976B1
Source datasetuspto-grants-2003_04
ORD IDord-72421745bf2e45eb972db3ffbc71cdf1
Source noteuspto-grants-2003_04