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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290773Generated: October 30, 2026

Sodium borohydride → HCID 13690970, compound

https://huagongshe.com/reaction/2290773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13690942HCID 13690942—
SolventEthanolHCID 702—
ProductHCID 13690970HCID 1369097096.5%

Reaction Steps

To a solution of 1.03 g of 5-[3-(4-biphenylyl)-3-oxopropyl]-3-chloromethyl-1,2,4-oxadiazole obtained in Example 3 in 100 ml of ethanol was added 0.12 g of sodium borohydride. After stirring for 10 minutes at room temperature, the reaction mixture was concentrated under reduced pressure. The residue was treated with ice-water and extracted with chloroform. The organic phase was washed with water, dried over sodium sulfate and evaporated to give 1.0 g of 5-[3-(4-biphenylyl)-3-hydroxypropyl]-3-chloromethyl-1,2,4-oxadiazole, m.p. 48°-49° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618617
Source datasetuspto-grants-1986_10
ORD IDord-56ed1a60574d40b594c2d97844036044
Source noteuspto-grants-1986_10