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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425291Generated: October 28, 2026

Hydrochloric Acid → 2,3-Dihydro-1-benzofuran-7-carbaldehyde

https://huagongshe.com/reaction/2425291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl chloroformateHCID 6586—
Reactant2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 2795014—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178418287HCID 178418287—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2,3-Dihydro-1-benzofuran-7-carbaldehydeHCID 279501860.7%

Reaction Steps

2,3-Dihydrobenzofuran-7-carboxylic acid (820 mg, 5 mmol) was dissolved in THF (10 mL). To the solution was added TEA (0.7 mL, 5 mmol) and methylchloroformate (0.43 mL, 5 mmol). The solution was stirred for 0.5 hour. The white precipitates were removed by filtration, the filtrate was added to a solution of NaBH4 (437 mg, 12.5 mmol) in H2O (5 mL). The resulting solution was stirred overnight. The reaction mixture was neutralized with 2 M aqueous HCl solution and then extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The crude alcohol was dissolved in DCM. To the solution was added PCC (1.83 g, 7.5 mmol). The mixture was stirred for 2 hours at room temperature and diluted with diethyl ether, then ether layers were decanted. Combined organic layer was filtered though a layer of Celite®. The filtrate was concentrated to give crude product. The crude was purified from column with 10% EtOAc/hexane to afford 450 mg of 2,3-dihydrobenzofuran-7-carbaldehyde as a slightly yellow solid. HPLC 4.3 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964624B1
Source datasetuspto-grants-2011_06
ORD IDord-40f8b410a12f409abe4946aa183909cb
Source noteuspto-grants-2011_06