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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726539Generated: October 28, 2026

Sodium borohydride → HCID 19706768, compound

https://huagongshe.com/reaction/726539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19706767HCID 19706767—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19706768HCID 19706768—

Reaction Steps

A stirred, ice-cooled solution of 2,2-difluoro-3-ethyl-3-trimethylsilyloxy-pentanal (1.45 g, 6.08 mmol) in THF (5 ml) and ethanol (15 ml) was treated with sodium borohydride (2.76 mg, 7.30 mmol). After 30 minutes the reaction mixture was partitioned between ethyl acetate and water, and the organic layer was washed with brine, dried over MgSO4 and concentrated. Flash chromatography (50 g silica gel; 10% EtOac in petroleum ether as eluant) afforded the title compound as a colourless oil, δ 0.15 (s, 9H), 1.36 (t, 6H), 2.48 (m, 1H), 3.93 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710142
Source datasetuspto-grants-1998_01
ORD IDord-93eaf3dae7c34b798e8f531bbf78f1ea
Source noteuspto-grants-1998_01