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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381688Generated: November 1, 2026

Benzoic Acid → HCID 54154833, compound

https://huagongshe.com/reaction/381688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant5-Chloro-α,α-dimethyl-2-thiophenemethanolHCID 79001600—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54154833HCID 54154833—

Reaction Steps

To a stirred solution of 1(S)2-(5-chloro-2-thienyl-1-hydroxy-1-methylethane (5.7 g) in tetrahydrofuran (100 mL) is added triphenylphosphine (5.34 g) and benzoic acid (2.49 g). Diethyl azodicarboxylate (3.22 mL) is added dropwise and the mixture stirred at room temperature for about 18 hours. The solvent is removed in vacuo. The residue is purified by flash chromatography, eluting with 30% hexanes in methylene chloride, to give (R)-3-(5-chloro-2-thienyl)-2-propyl benzoate. The ester (3.91 g) is dissolved in dioxane (50 mL) and 20% aqueous sodium hydroxide (15 mL) is added. The mixture is heated at 55° C. for 3 hours and concentrated in vacuo. The residue is taken up in ethyl acetate (200 mL) and the organic layer washed with brine, dried over magnesium sulfate, filtered, concentrated in vacuo to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307054B1
Source datasetuspto-grants-2001_10
ORD IDord-22bc893539424840ae92c0c60430b588
Source noteuspto-grants-2001_10