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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727573Generated: October 30, 2026

1-Bromo-2-Chloroethane → HCID 19705538, compound

https://huagongshe.com/reaction/727573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 54070984HCID 54070984—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19705538HCID 19705538—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A cold (-78° C.) solution of tert-butyl 2-oxo-1-(2-phenylethyl)-3-(propen-2-yl)-3-pyrrolidineacetate (prepared similarly to that described in EXAMPLE 1, step 3; 5.52 g, 16.1 mmol) in dry THF (100 mL) is treated with the dropwise addition of LDA (9.66 mL, 19.3 mmol, 2.0N). The solution is stirred for 30 min, and then treated with the dropwise addition of 1-bromo-2-chloroethane (1.61 mL, 19.3 mmol). The solution is maintained at -78° C. for 5 hours and then allowed to slowly warm to room temperature under N2 overnight. The solution is quenched with saturated NH4Cl (10 mL) and diluted with H2O (25 mL). The product is extracted with EtOAc (3×100 mL), dried over anhydrous MgSO4, filtered, and concentrated to give 6.6 g of a brown oil. The oil is purified by silica gel chromatography (275 g SG; 10% EtOAc/hexane) to provide 5.07 g (78%) of the title compound as a clear, yellow oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712300
Source datasetuspto-grants-1998_01
ORD IDord-9f164a419ca84ce9b3014d080076bbec
Source noteuspto-grants-1998_01