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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891801Generated: October 29, 2026

3-Hydroxyazetidine → HCID 86590882, compound

https://huagongshe.com/reaction/891801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxyazetidineHCID 1514290—
ReactantHCID 86590883HCID 86590883—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86590882HCID 8659088261%

Reaction Steps

To a solution of 3-(t-butyldiphenylsilyloxy)-2-isothiocyanatopropionic acid methyl ester (13.4 g, 33.5 mmol) (obtained as described in Reference Example 70(1)) in tetrahydrofuran (245 ml) was added a solution of 3-hydroxyazetidine (4.90 g, 67.1 mmol) (obtained as described in Reference Example 31(1)) in water (50 ml) at room temperature and the mixture was stirred overnight. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using toluene and toluene:acetonitrile (3:1) as the eluant to afford (2S)-3-(t-butyldiphenylsilyloxy)-2-[(3-hydroxyazetidine-1-carbothioyl)amino]propionic acid methyl ester (9.60 g, yield 61%) as an yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-ae3948d98d2e441e84fa584781c0593c
Source noteuspto-grants-2006_02