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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350993Generated: October 25, 2026

Triphenylphosphine → HCID 60128036, compound

https://huagongshe.com/reaction/350993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant2-Fluoro-4-hydroxybenzonitrileHCID 2734675—
Reactantmethyl (2S)-3-hydroxy-2-methylpropanoateHCID 10192563—
SolventEthyl AcetateHCID 8857—
ProductHCID 60128036HCID 601280368.1%

Reaction Steps

To a stirred solution of 2-fluoro-4-hydroxybenzonitrile (1.0 g, 7.3 mmol), (S)-3-hydroxy-2-methyl-propionic acid methyl ester (0.8 mL, 7.3 mmol) and triphenylphosphine (2.3 g, 8.8 mmol) at room temperature, diethyl azodicarboxylate (1.4 mL, 8.8 mmol) was added dropwise. The mixture was stirred at room temperature overnight, diluted with ethyl acetate and washed successively with dilute aqueous sodium hydroxide, dilute aqueous hydrochloric acid, brine, and dried (MgSO4). Solvents were stripped in vacuo. The resulting oil was washed with diethyl ether and the precipitate was filtered off. The mother liquor was adsorbed onto silica gel and the product purified by flash column chromatography (40% ethyl acetate/hexane), affording 0.14 g of a yellow oil (8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183293B2
Source datasetuspto-grants-2007_02
ORD IDord-4c9fa0b8cba6460498c48c0c63c8ad7d
Source noteuspto-grants-2007_02