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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380054Generated: November 4, 2026

Sodium borohydride → HCID 14685621, compound

https://huagongshe.com/reaction/1380054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-Chloro-2-pyrimidinyl)benzaldehydeHCID 13590378—
SolventIsopropanolHCID 3776—
ProductHCID 14685621HCID 14685621—

Reaction Steps

A 1.0 g portion of 3-(4-chloro-2-pyrimidinyl)benzaldehyde was dissolved in 230 ml of 2-propanol and 0.32 g of freshly ground sodium borohydride pellets was added. After stirring for 3 hours at 50°-60° C. in a water bath, the excess reducing agent was destroyed with 6N hydrochloric acid. The solution was neutralized with sodium bicarbonate and the mixture concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and then evaporated, giving 1.1 g of the desired intermediate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579848
Source datasetuspto-grants-1986_04
ORD IDord-d725d9425e744f0d9357d97130488c10
Source noteuspto-grants-1986_04