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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739413Generated: October 28, 2026

Sodium borohydride → HCID 54384770, compound

https://huagongshe.com/reaction/1739413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21841070HCID 21841070—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 54384770HCID 5438477053.8%

Reaction Steps

1.2 g of 4-(3-phenylthiopropyloxy)benzaldehyde were dissolved in 30 ml of ethanol, and the resultant solution was further added with 0.08 g of sodium borohydride and then stirred for 1 hour at room temperature. After completed the reaction, the solvent used was removed by distillation under reduced pressure, and the residue obtained was dissolved in a mixture of ethyl acetate and dilute hydrochloric acid. The ethyl acetate layer resulted was then washed with dilute hydrochloric acid, aqueous solution of sodium hydroxide and water in series. The organic layer resulted was then dried with anhydrous magnesium sulfate, and the solvent used was removed by distillation under reduced pressure, thereby affording 0.65 g of 4-(3-phenylthiopropyloxy)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965743
Source datasetuspto-grants-1999_10
ORD IDord-d2677323cadb4d60abc978ff4b1e37d8
Source noteuspto-grants-1999_10