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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568071Generated: October 29, 2026

Methanol → HCID 54386099, compound

https://huagongshe.com/reaction/568071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 54478229HCID 54478229—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54386099HCID 5438609996.3%

Reaction Steps

15.5 ml (0.155 mol) of borane/methyl sulphide complex are added dropwise to a solution of 31.5 g (0.0775 mol) of 3-ethoxycarbonyl-4-(3-fluorophenyl)-4-(4-methanesulphonylphenyl)-3-butenoic acid, prepared in Example 11, in 90 ml of anhydrous tetrahydrofuran. The mixture is stirred at room temperature for 8 hours and 23.5 ml of methanol are added dropwise. The mixture is evaporated to dryness under vacuum and the residue is taken up with ethyl acetate and then treated with an aqueous solution of 7.6 g of potassium carbonate. The organic phase is decanted and then dried over magnesium sulphate and evaporated to dryness under vacuum to give 29.3 g of ethyl 3-(3-fluorophenyl)-3-(4-methanesulphonylphenyl)-2-(2-hydroxyethyl)-2-propenoate in the form of a viscous oil, which is used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180651B2
Source datasetuspto-grants-2001_01
ORD IDord-8ee6ae842bd14c4bbcf21b3aeef8c5fa
Source noteuspto-grants-2001_01