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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120907Generated: October 30, 2026

Hydrochloric Acid → (7-Methoxy-1,3-benzodioxol-5-yl)methanol

https://huagongshe.com/reaction/2120907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 3,4-methylenedioxy-5-methoxybenzoateHCID 601780—
ReactantEthyl acetate hexaneHCID 21226206—
SolventTetrahydrofuranHCID 8028—
Product(7-Methoxy-1,3-benzodioxol-5-yl)methanolHCID 60266788%

Reaction Steps

Methyl 7-methoxybenzo[3,4-d]1,3-dioxolane-5-carboxylate(10 g, 47.57 mmol) prepared in Step 3 was dissolved in tetrahydrofuran(200 ml), borane methylsulfide(BMS, 10M) (9.5 ml, 95.0 mmol) was added thereto, and the mixture was stirred under reflux for 1.5 hour. The reaction vessel was cooled down to room temperature and the reaction mixture was neutralized to pH 6-7 using 1N—HCl at 0-5° C., which was then extracted with ethyl acetate. The extract was washed with saturated saline solution, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/2, v/v) to give (7-methoxybenzo[3,4-d]1,3-dioxolan-5-yl)methan-1-ol(7.63 g, Yield 88%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693126B2
Source datasetuspto-grants-2004_02
ORD IDord-62f7d0df5d624a348982cb5594475059
Source noteuspto-grants-2004_02