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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911501Generated: October 30, 2026

1,2-Dibromoethane → HCID 68712528, compound

https://huagongshe.com/reaction/1911501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 59323878HCID 59323878—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68712528HCID 68712528—

Reaction Conditions

Temperature-55 °C

Reaction Steps

A solution of lithium diisopropylamide in THF (2 M, 5.05 ml) was cooled to −55° C. and treated with (RS)-4-(2,4-difluoro-phenyl)-4,5-dihydro-oxazol-2-ylamine (667 mg, example 7) in THF (6 ml). The reaction mixture was stirred at −55° C. for 2 hrs, then treated dropwise with 1,2-dibromoethane (0.58 ml). The reaction mixture was warmed to r.t., then stirred overnight at r.t. It was quenched with H2O and extracted with EtOAc. The organic layer was dried over MgSO4, filtrated and concentrated. The crude product was purified by column chromatography (SiO2; gradient: CH2Cl2->CH2Cl2/MeOH 95:5) to give (RS)-4-(3-bromo-2,4-difluoro-phenyl)-4,5-dihydro-oxazol-2-ylamine (61 mg) as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-8308a1e5d9464f09b5bd6808417beed6
Source noteuspto-grants-2013_12