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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046395Generated: November 3, 2026

Sodium Fluoride → HCID 58046435, compound

https://huagongshe.com/reaction/2046395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FluorideHCID 5235—
Reactant1-Phenethylamine, (+)-HCID 643189—
ReactantTrimethylaluminumHCID 16682925—
Reactant2,2-Difluoro-7-oxabicyclo[4.1.0]heptaneHCID 53402014—
SolventDichloromethaneHCID 6344—
ProductHCID 58046435HCID 58046435—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (1R)-1-phenylethanamine (72 mL, 0.57 mol) in dichloromethane (200 mL) was cooled to 0° C. and treated with trimethylaluminum (260 mL, 0.52 mol) and the resulting solution was stirred for 1 hour at 0° C. To this solution was added a solution of 2,2-difluoro-7-oxabicyclo[4.1.0]heptane (66 g, 0.49 mol) in dichloromethane (200 mL) and the resulting mixture stirred at 0° C. for 3 hours. The reaction was then warmed to ambient temperature for 16 hours. The reaction was cooled to 0° C., treated with 103 g of sodium fluoride and then quenched with water (90 mL, slow addition). The reaction was warmed to ambient temperature, the solids filtered and the solution evaporated in vacuo. Purification by flash chromatography afforded the title compound as a white solid: 1H NMR (500 MHz, CDCl3) δ 7.32 (s, 5H); 3.90 (q, 1H); 3.39 (ddd, 1H); 2.70 (m, 1H); 2.11 (m, 1H); 1.80 (m, 1H); 1.62 (m, 2H); 1.43 (m, 1H); 1.36 (d, 3H); 0.96 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592425B2
Source datasetuspto-grants-2013_11
ORD IDord-b43f6acbf4e548e9a14a6e1f7e7cbd69
Source noteuspto-grants-2013_11