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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898847Generated: October 30, 2026

Hexane → HCID 60039216, compound

https://huagongshe.com/reaction/898847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDi-tert-butyl malonateHCID 68324—
Reactant2-(Chloromethyl)-2-phenyloxiraneHCID 200204—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 60039216HCID 6003921661.5%

Reaction Steps

Under nitrogen atmosphere, potassium t-butoxide (110 g, 0.78 mol) was added to a solution of di-t-butyl malonate (170 g, 0.78 mol) in t-butyl alcohol (1.5 L) in 3 portions at room temperature. After stirring at room temperature for 1 hour, the mixture was heated to 70° C. Then a solution of 2-chloromethyl-2-phenyloxirane (120 g) in tetrahydrofuran (500 mL) synthesized by the method described in J. Org. Chem. (1962, 27, 2241-2243) was added dropwise over 90 min. After stirring for 12 hours at 70° C., the mixture was cooled to room temperature and the solvent was evaporated. 10% Aqueous citric acid solution (500 mL) was added to the residue. The mixture was extracted with ethyl acetate (2.0 L), sequentially washed with water (500 mL) and saturated aqueous sodium chloride solution (200 mL), and dried over magnesium sulfate. After filtration and evaporation, the title compound (120 g, 3 step, yield 54%) was recrystallized from a mixed solution of hexane:diisopropyl ether=1:1 (600 mL) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351825B2
Source datasetuspto-grants-2008_04
ORD IDord-e4755ddd317d41efba754e88f51471fc
Source noteuspto-grants-2008_04