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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655362Generated: November 1, 2026

1-Bromo-2-Chloroethane → HCID 23001007, compound

https://huagongshe.com/reaction/1655362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl cyclohexylacetateHCID 21595—
Reactantn-Butyl lithiumHCID 61028—
Reactant2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23001007HCID 23001007—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Diisopropylamine (2.71 ml, 1.1 eq.) was added to dry THF (10 ml) and cooled to -78° C. N-Butyllithium (11.01 ml of 1.6 Molar solution, 1.0 eq.) was added and the mixture stirred at -78° C. for 0.5 hour. To this mixture was then added dropwise a solution of ethyl-2-cyclohexylacetate (3.0 g, 1.0 eq.) in THF (20 ml) at -78° C. and stirred for 0.5 hour. DMPU (2.13 ml, 1.0 eq.) in THF (20 ml) was added dropwise and allowed to stir at -78° C. for 10 minutes. To this mixture was added 1-bromo-2-chloroethane (1.46 ml, 1.0 eq.) in THF (10 ml) and the mixture stirred at -5° C. for 15 minutes. The mixture was then warmed to room temperature and stirred for 1.0 hour. The mixture was cooled to 0° C., quenched with saturated ammonium chloride solution, extracted with ethyl ether and the ether layer was washed three times with water. The organic layer was separated, dried over K2CO3 and the solvent removed to provide 3.6 g of product. This was fractionally distilled to provide 3.0 g of product Boiling Point 66°-70° C. at 0.05 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250542
Source datasetuspto-grants-1993_10
ORD IDord-b21afd45fa134ba6a1445fa76a415371
Source noteuspto-grants-1993_10