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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721238Generated: November 2, 2026

Triethylamine → HCID 54294220, compound

https://huagongshe.com/reaction/1721238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl acrylateHCID 15458—
ReactantHCID 14560581HCID 14560581—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 54294220HCID 5429422054%

Reaction Conditions

Temperature90 °C

Reaction Steps

Bis(triphenylphosphine) palladium dichloride (120 mg, 0.2 mm, 1) was added to a deoxygenated mixture of (S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-3-[4-[[(trifluoromethyl)sulfonyl ]oxy]phenyl]propanoic acid diphenylmethyl ester (3.0 g 0 5.2 mmol), t-butyl acrylate (1.5 mL, 10.2 mmol) and triethylamine (4.0 mL 30.0 mmol) in DMF (50 mL) and the well-stirred suspension was then heated at 90° C. (24 h). The solvent was removed in vacuo and the resulting residue was purified by flash chromatography on silica gel eluting with a mixture of dichloromethane and hexanes (8:1) to give the (S)-2-[[(1,1-dimethylethoxy) carbonyl]amino]-3-[4-[3-(1,1-dimethylethoxy)-3-oxo-1-propenyl]phenyl]propanoic acid diphenylmethyl ester (1.6 g, 2.8 mmol) in 54% yield, mp. 135°-137° C., [α]D -5.35° (0.97% in ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508437
Source datasetuspto-grants-1996_04
ORD IDord-952774a6a41f4b8d9ef5965020d9cf3b
Source noteuspto-grants-1996_04