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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49243Generated: October 28, 2026

Potassium Carbonate → [8-Methyl-2,3-dihydrofuro[3,2-f][1,4]benzodioxin-2-yl]methanol

https://huagongshe.com/reaction/49243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3S)-5-(2-chloro-2-propenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-olHCID 86586531—
SolventTrifluoroacetic acidHCID 6422—
Product[8-Methyl-2,3-dihydrofuro[3,2-f][1,4]benzodioxin-2-yl]methanolHCID 18546026—

Reaction Steps

A solution of 0.40 g (1.6 mmole) of (3S)-5-(2-chloro-2-propenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-ol in 70 mL of trifluoroacetic acid was stirred at room temperature for 26 hours. The solvent was then removed in vacuum and replaced with 100 mL of methanol. Potassium carbonate (3.0 g, 2.2 mmole) was added and the mixture stirred for an additional 1.5 hours at room temperature. The mixture was then filtered and the filtrate concentrated to a brown residue in vacuum. The residue was column chromatographed on silica gel with methylene chloride as eluant to give 0.20 g (60%) of the (S)-enantiomer of the title compound as a yellow oil. 1H-NMR (d6-DMSO): doublet 6.94 δ (1H); doublet 6.71 δ (1H); singlet 6.48 δ (1H); triplet 5.07 δ (1H); doublet of doublets 4.30 δ (1H); multiplet 4.22 δ (1H); multiplet 4.00 δ (1H); multiplet 3.65 δ (2H); singlet 2.38 δ (3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706736B2
Source datasetuspto-grants-2004_03
ORD IDord-d12f1a3742514410befd9a66309986c4
Source noteuspto-grants-2004_03