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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412163Generated: October 26, 2026

Sodium borohydride → 1,4-Di-[(methanesulfonyl)oxy]-2-(hydroxymethyl)benzene

https://huagongshe.com/reaction/412163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2.5-Di-[(methanesulfonyl)oxy]benzaldehydeHCID 18536186—
SolventTetrahydrofuran ethanolHCID 21873804—
Product1,4-Di-[(methanesulfonyl)oxy]-2-(hydroxymethyl)benzeneHCID 18536045—

Reaction Steps

To a solution of the product from Step A (17.13 g, 58.2 mmol) in 150 mL of 2:1 THF/ethanol at 0° C. was added sodium borohydride (2.27 g, 60.0 mmol). After 30 minutes, the reaction was carefully quenched by the addition oc saturated NH4Cl solution, then partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The product was isolated as a yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562823B1
Source datasetuspto-grants-2003_05
ORD IDord-af8b38658e2845c38b40455500b14b75
Source noteuspto-grants-2003_05