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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454770Generated: October 30, 2026

1,2-Dichloroethane → HCID 68864647, compound

https://huagongshe.com/reaction/1454770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant(+-)-alpha-PineneHCID 6654—
ReactantHCID 3015793HCID 3015793—
CatalystZincchlorideHCID 3007855—
ProductHCID 68864647HCID 688646477.1%

Reaction Steps

Method a) A mixture of 11.81 g 2-methyl-but-2-enoyl chloride (0.10 mol) and 1.36 g zinc chloride (0.01 mol, 0.1 eq.) in 100 ml ethylene chloride was treated with a soln. of 136 g α-pinene ((1S)-(−)/(1R)-(+) 90:10, 1 mol, 10 eq.) in 150 ml ethylene chloride and the resulting mixture was stirred 45 min. at 25° C., 2.5 h at 50° C., and 1 h at 80°. After cooling, the reaction mixture was washed with aq. sat. NaCl soln. and aq. sat. NaHCO3 soln. The aq. phases were extracted with Et2O, dried (Na2SO4), and concentrated. The crude product (48 g) filtered (SiO2, hexane/Et2O 200:6→200:13) and the residue (5.1 g) treated with 1 g LiOH.H2O in 75 ml MeOH at 25° C. for 48 h. The resulting mixture was poured into aq. sat. NaCl soln. and extracted with hexane. The combined org. phases were dried (Na2SO4), concentrated and purified by FC (SiO2, hexane/Et2O 100:3) gave 1.6 g (7.1%) of compound 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482313B2
Source datasetuspto-grants-2009_01
ORD IDord-cf57c8374f6c41d8af043789165f1530
Source noteuspto-grants-2009_01