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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243282Generated: November 1, 2026

tert-Butyl ((S)-2-(3,5-difluorophenyl)-1-((R)-oxiran-2-yl)ethyl)carbamate → HCID 12988679, compound

https://huagongshe.com/reaction/1243282

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl ((S)-2-(3,5-difluorophenyl)-1-((R)-oxiran-2-yl)ethyl)carbamateHCID 11415322—
ReactantHCID 12988678HCID 12988678—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12988679HCID 12988679—

Reaction Conditions

Temperature-78 °C

Reaction Steps

(1S,2S)-[2-(3,5-Difluorophenyl)-1-oxiranylethyl]-carbamic acid tert-butyl ester (VI, 113 mg) and 1-((3aS,8aR)-2,2-Dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-butan-1-one (VII, 94 mg) were combined in dry THF (3 mL), and cooled to −78° C. To this solution was added BuLi (2.5 M in hexanes, 0.32 mL) over 5 min., whereupon the solution was allowed to warm to 0° C. for 1.5 h. The reaction mixture was partitioned between 0.5 N HCl (4 mL) and 1:1 EtOAc/hexanes (2×4 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography (20–30% EtOAc/hexanes) to give an oil: MH+559.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119085B2
Source datasetuspto-grants-2006_10
ORD IDord-4b0ced2d6a784e76a0c683e9eb357be8
Source noteuspto-grants-2006_10