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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119984Generated: October 30, 2026

HCID 131724336, compound → HCID 131724337, compound

https://huagongshe.com/reaction/2119984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131724336HCID 131724336—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 131724337HCID 13172433773.3%

Reaction Steps

A solution of 4-(2-nitro-phenyl)-4-trimethlysilanyloxy-butyric acid ethyl ester (200 mg, 0.6 mmol) in dry EtOAc (5 mL) was hydrogenated (1 atm) in the presence of Pd/C (20 mg) overnight Then the mixture was filtered and evaporated. The residue was dissolve in dry MeOH (5 mL) and was further hydrogenated (1 atm) in the presence of Pd/C (20 mg) for 1 h. The mixture was then filtered and the filtrate evaporated. Purification of this residue by filtration over silica gel, eluting with hexane: ethyl acetate (8:1) afforded the title compound (130 mg, 72%) as a colorless oil; m/z 295 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686352B2
Source datasetuspto-grants-2004_02
ORD IDord-102edcbbae1c46e2955778d7a6b6fad7
Source noteuspto-grants-2004_02