Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440409Generated: October 29, 2026

tert-Butyl hydroperoxide → (2R-trans)-3-[3-(1-Dodecynyl)pbenyl]oxiranemethanol

https://huagongshe.com/reaction/440409

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
Reactanttrans-3-[3-(1-Dodecynyl)phenyl]propen-1-olHCID 18372907—
Reactant(+)-DiisopropyltartrateHCID 21909808—
CatalystTitanium isopropoxideHCID 11026—
SolventDichloromethaneHCID 6344—
Product(2R-trans)-3-[3-(1-Dodecynyl)pbenyl]oxiranemethanolHCID 18656053916.1%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution (-) diisopropyltartrate (524 mg) in dry dichloromethane (60 ml) and 4A molecular sieves (1 g) at -20° C. was added titanium(IV) isopropoxide (0.53 ml) followed by t-butylhydroperoxide (3.0M, isooctane) (20 ml). The reaction mixture was stirred for 20 mins at -20° C. and then a solution of trans-3-[3-(1-dodecynyl)phenyl]propene-1-ol (8.88 g) in dichloromethane (20 ml) was added slowly. The mixture was stirred for 1.5 hr and quenched with 25% aqueous sodium hydroxide (6 ml) followed by water (40 ml). The mixture was allowed to warm to room temperature, and was stirred for 30 min. The organic phase was separated, and the aqueous phase was extracted with dichloromethane. The organic extracts were combined, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed over silica gel (eluted with ethyl acetate/Heptane/1:2). The appropriate fractions were collected and evaporated. The residue was crystallized from heptane to afford 6.5 g (69%) of product, mp 41°-42° C. [α]D25 +33.1° (c. 0.725, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519062
Source datasetuspto-grants-1996_05
ORD IDord-804f5b19c41b4c1383822f7908e40aff
Source noteuspto-grants-1996_05