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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894148Generated: November 1, 2026

HCID 178454090, compound → HCID 178454089, compound

https://huagongshe.com/reaction/1894148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178454090HCID 178454090—
SolventDichloromethaneHCID 6344—
ProductHCID 178454089HCID 178454089100.4%

Reaction Steps

To a solution of trans-(3-hydroxymethyl-cyclobutyl)-carbamic acid tert-butyl ester (Compound 4a) (0.2 g; 1.0 mmol) in anhydrous dichloromethane (8.0 mL) at 0° C. was added 1,1,1-tris(acetyloxy)-1,1-dihydro-1,2-benzodioxol-3-(1H)-one (0.84 g; 2.0 mmol). The reaction was allowed to stir at room temperature under nitrogen for 3 h, before partitioning the reaction mixture between dichloromethane and brine. The organic layer was washed with brine, dried over Na2SO4, filtered, and the solvent evaporated in vacuo to yield a crude oil. The crude oil was purified via flash column chromatography, eluting with 30% ethyl acetate in hexanes, to yield Compound 4b as a foam (0.2 g; 88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513271B2
Source datasetuspto-grants-2013_08
ORD IDord-ea9f10a0f8cb45728906560157d44137
Source noteuspto-grants-2013_08