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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739409Generated: October 31, 2026

Sodium borohydride → HCID 54058846, compound

https://huagongshe.com/reaction/1739409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15871016HCID 15871016—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 54058846HCID 5405884682.8%

Reaction Steps

1.8 g of 4-(3-benzenesulfonylpropyloxy)benzaldehyde were dissolved in 30 ml of ethanol, and the resultant solution was further added with 0.11 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 1.5 g of 4-(3-benzenesulfonylpropyloxy)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965743
Source datasetuspto-grants-1999_10
ORD IDord-8c3eb55009d847ac9a80080db457ad04
Source noteuspto-grants-1999_10