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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478937Generated: November 4, 2026

Ammonium Chloride → 1-Benzofuran-5-ylmethanol

https://huagongshe.com/reaction/1478937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Benzofuran-5-carbaldehydeHCID 2773875—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product1-Benzofuran-5-ylmethanolHCID 2795179100%

Reaction Steps

A solution of 5-benzofurancarboxaldehyde (10 g, 68 mmol) in MeOH (40 mL) was cooled in an ice bath. NaBH4 (3.84 g, 102 mmol) was added over a period of 2 hr and stirring continued for 20 min. Saturated NH4Cl was added. The mixture was suspended in ethyl acetate (100 mL) and the solid was filtered off. The solution was concentrated, partitioned between ethyl acetate and brine, dried over anhydrous Na2SO4, concentrated and dried under high vacuum to furnish benzofuran-5-ylmethanol (10 g, 100%) as a solid, which was taken up in CH2Cl2 (60 mL) to which SOCl2 (5.9 mL, 81 mmol) was added at room temperature. The reaction mixture was stirred for 3 hr. The reaction mixture was diluted with CH2Cl2, washed with a saturated solution of NaHCO3, then brine, dried over anhydrous Na2SO4, and concentrated in vacuo to furnish 5-chloromethylbenzofuran (10 g, 90%) as an oil. This material was used without further purification to synthesize D-benzofurylalanine according to C. Behrens, Tetrahedron 56 (2000), 9443-9449.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403789B2
Source datasetuspto-grants-2016_08
ORD IDord-f9b7be7a343b4e2da948bffc3ef74e4c
Source noteuspto-grants-2016_08