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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907039Generated: October 29, 2026

Dioxane sulfuric acid → 5-(Hydroxymethyl)-1,3-dihydro-2-benzofuran-1-one

https://huagongshe.com/reaction/1907039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDioxane sulfuric acidHCID 19613996—
ReactantHCID 67127237HCID 67127237—
SolventDichloromethaneHCID 6344—
Product5-(Hydroxymethyl)-1,3-dihydro-2-benzofuran-1-oneHCID 12446860—

Reaction Steps

A suspension of 2 (22.1 g, 65.7 mmol) in 700 mL of a 1:1 mixture of dioxane/sulfuric acid (1M) was heated under reflux for 20 h. After cooling to room temperature, the mixture was poured into 200 mL of DCM. The phases were separated and the aqueous phase was extracted with DCM (5×200 mL). The combined organic layers were washed with saturated NaHCO3 (3×200 mL) and brine (1×200 mL) and were dried over MgSO4. The solvent was removed in vacuo to yield 8.70 g (83%) of pure 3 as a colorless solid: 1H-NMR (400 MHz, DMSO-d6): δ 4.65 (s, 2H), 5.39 (s, 2H), 5.47 (br s, 1H), 7.51 (d, J=7.8 Hz, 1H), 7.60 (s, 1H), 7.78 (d, J=7.7 Hz, 1H); 13C-NMR (100 MHz, DMSO-d6): δ 62.4, 69.7, 120.0, 123.3, 124.5, 126.9, 147.5, 149.7, 170.5; MS (Cl+ (NH3)) m/z=165.0 (M+H+, 100), 182.0 (M+NH4+, 49).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08597631B2
Source datasetuspto-grants-2013_12
ORD IDord-384d6b62a4854af68aaad86cd757b8e7
Source noteuspto-grants-2013_12