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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053715Generated: November 2, 2026

Hydrochloric Acid → 3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acid

https://huagongshe.com/reaction/1053715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl esterHCID 25129046—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acidHCID 25129047105.5%

Reaction Steps

A mixture of 3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl ester (300 mg, 1.06 mmol) obtained in Example 4(B), sodium hydroxide (260 mg, 6.5 mmol), ethanol (10 ml) and water (1 ml) in tetrahydrofuran (10 ml), is stirred for 12 h at room temperature. The reaction medium is acidified by adding a 1.2 M hydrochloric acid solution and extracted with ethyl acetate. The organic phase is washed with water, dried (Na2SO4), and concentrated in a rotary evaporator. The product is obtained as a white solid (300 mg, 100%). Mp: 165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394267B2
Source datasetuspto-grants-2016_07
ORD IDord-7a3e2f1359e14384b23bfd7ef30a5173
Source noteuspto-grants-2016_07