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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662559Generated: October 30, 2026

1,2-Ethanedithiol → Methyl 3-(3-hydroxyphenyl)-3-methylbutanoate

https://huagongshe.com/reaction/1662559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-EthanedithiolHCID 10902—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantMethyl 3-(3-methoxyphenyl)-3-methylbutanoateHCID 57705813—
Solvent1,2-DichloroethaneHCID 11—
ProductMethyl 3-(3-hydroxyphenyl)-3-methylbutanoateHCID 5770615898.4%

Reaction Steps

To a solution of methyl 3-(3-methoxyphenyl)-3-methylbutanoate 85.E (0.227 g, 1.02 mmol) in 1,2-dichloroethane (10 mL) was added 1,2-ethanedithiol (1.37 mL, 16.3 mmol) followed by aluminum chloride (1.09 g, 8.17 mmol) at 0° C. The reaction mixture was allowed to slowly warm to room temperature over four hours and was then quenched with saturated Rochelle's salt (potassium sodium tartrate) solution. The mixture was extracted (2×50 mL) with DCM. The combined organic layers were washed with water (1×40 mL) and brine (1×40 mL) and dried over magnesium sulfate. The filtrate was concentrated and the residue was purified by medium pressure chromatography (silica, 0 to 30% EtOAc:hexanes) to give methyl 3-(3-hydroxyphenyl)-3-methylbutanoate 85 (0.209 g, 98.3% yield). MS ESI (pos.) m/e: 226.0 (M+H2O)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-d8f1041ae3da493ebb8cfbf1257ad20c
Source noteuspto-grants-2011_10