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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357404Generated: October 30, 2026

Hydrogen Peroxide → HCID 69507241, compound

https://huagongshe.com/reaction/1357404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantDiethyl EtherHCID 3283—
ReactantPentaneHCID 8003—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131723665HCID 131723665—
ProductHCID 69507241HCID 69507241—

Reaction Conditions

Temperature-50 °C

Reaction Steps

A solution of 2-methyl-3-(2-((2,2,2-trichloroethoxycarbonyloxymethyl)thiazol-4-yl)propenal (9.20 g) in 50 mL of anhydrous ether is cooled to −100° C. A pentane solution of (+)-diisopinocampheylallylborane (1.5 equiv) is added dropwise to the vigorously stirred aldehyde solution. After the addition is complete, the reaction mixture is stirred for 1.5 hours and warmed to −50° C. A solution of 30% aq H2O2 (20 mL) and 10% aq NaHCO3 (50 mL) is added, and the resulting turbid mixture is stirred at 25° C. for 8 hours. The organic layer is separated, and the aqueous layer is extracted with ether. The combined organic layers are washed with satd aq Na2S2O3 and brine, dried (MgSO4), filtered, and concentrated. Purification by flash column chromatography on SiO2 (hexanes/ethyl acetate, 10:1) affords the alcohol as a clear oil (7.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589968B2
Source datasetuspto-grants-2003_07
ORD IDord-22b3e375b9014c97937a6e08acbc19ff
Source noteuspto-grants-2003_07