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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284854Generated: November 3, 2026

Sodium borohydride → HCID 118114326, compound

https://huagongshe.com/reaction/2284854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 4378040HCID 4378040—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118114326HCID 11811432696.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl 5-((4-benzoylphenoxy)methyl)furan-2-carboxylate (330 mg, 1.0 mmol) in methanol (5 mL) and THF (5 mL) was cooled to 0° C. NaBH4 (58 mg, 1.53 mmol) was added in one portion and the reaction was stirred at 0° C. for 2 hours. The reaction was quenched by addition of water (0.75 mL). The mixture was stirred for 10 minutes and the majority of the solvent was removed in vacuo. The residue was partitioned between EtOAc and water and the aqueous phase was extracted twice with EtOAc. The combined organic phases were washed with brine, dried over MgSO4, filtered and the solvent was removed in vacuo to give the title compound (325 mg, 96.1%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145409B2
Source datasetuspto-grants-2015_09
ORD IDord-c9e0a7b56ac5477f8aa60408072c2b69
Source noteuspto-grants-2015_09