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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780047Generated: November 1, 2026

Hydrogen Peroxide → HCID 15870214, compound

https://huagongshe.com/reaction/1780047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantDimethyl SulfideHCID 1068—
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10824826HCID 10824826—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15870214HCID 1587021482%

Reaction Steps

To a suspension of sodium borohydride (1.78 g) in tetrahydrofuran (70 ml)is added dimethylsulfide (2.8 ml) at room temperature, and thereto is added dropwise a solution of boron trifluoride·ether complex (6.3 ml) in tetrahydrofuran (10 ml) at room temperature, and the mixture is stirred for 30 minutes. To the mixture is added (3R)-3-benzylthio-3-carboxypropionic acid methyl ester (10 g) at room temperature, and the mixture is stirred for 1.5 hour. After the reaction is completed, to the reaction solution are added successively 2N aqueous sodium hydroxide solution (16 ml), 30% aqueous hydrogen peroxide solution (11 ml), and then further added a saturated aqueous sodium chloride solution. The mixture is extracted with chloroform, and the extract is dried, concentrated under reduced pressure, and the residue is purified by silica gel column chromatography (solvent; n-hexane:ethyl acetate=2:1) to give (3R)-3-benzylthio-4-hydroxybutyric acid methyl ester (7.75 g) as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629419
Source datasetuspto-grants-1997_05
ORD IDord-a8e4e6fcd8f14bcc9cedcf551546834c
Source noteuspto-grants-1997_05