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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978460Generated: October 29, 2026

Sodium borohydride → HCID 20203303, compound

https://huagongshe.com/reaction/978460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12477271HCID 12477271—
SolventEthanolHCID 702—
ProductHCID 20203303HCID 2020330393.8%

Reaction Steps

2-(4-Oxopentyl)thiophene (3.30 g, 19.6 mmol) was dissolved in 10 ml of 95% ethanol and the solution was added to a stirred solution of sodium borohydride (0.38 g, 10 mmol) in 20 ml of ethanol at room temperature. The mixture was stirred overnight and the excess reducing agent destroyed by the dropwise addition of 1N HCl. The solvents were evaporated and the residue partitioned between water and ether. The organic phase was washed with water and brine and dried (Na2SO4) Evaporation of the solvents gave 3.13 g of product as a yellow oil, which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665090
Source datasetuspto-grants-1987_05
ORD IDord-ced00bfdcd9c41c4a727bc81d7eeaaf7
Source noteuspto-grants-1987_05