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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235252Generated: October 31, 2026

Lithium diisopropylamide → HCID 68469023, compound

https://huagongshe.com/reaction/2235252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-Chloro-6-fluorobenzyl bromideHCID 2773625—
ReactantHCID 68468485HCID 68468485—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68469023HCID 68469023100.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve (4S,5R)-3-pent-4-enoyl-4,5-diphenyloxazolidin-2-one (1.0 g, 3.1 mmol) in THF (50 mL) and cool the mixture to −78° C. under N2 with stirring. Add dropwise LDA (2.7 mL, 4.0 mmol, 1.5 M in THF) and stir the mixture for 0.5 hours. Then add 2-(bromomethyl)-1-chloro-3-fluorobenzene (1.39 g, 6.22 mmol). Continue to stir the reaction mixture for one hour until TLC shows that the starting material has been consumed. Add water (50 mL) and extract the aqueous with CH2Cl2 (3×250 mL). Combine the organic layers and dry over Na2SO4. Concentrate and purify by chromatography (Silica gel) to afford (4S,5R)-3-((R)-2-(2-Chloro-6-fluorobenzyl)pent-4-enoyl)-4,5-diphenyloxazolidin-2-one (1.44 g, 75.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713979B2
Source datasetuspto-grants-2010_05
ORD IDord-23f4936e01c345c0abc5a5d3f2123aea
Source noteuspto-grants-2010_05