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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 54070984 | HCID 54070984 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19705538 | HCID 19705538 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05712300 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-9f164a419ca84ce9b3014d080076bbec |
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| Source note | uspto-grants-1998_01 |
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