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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045829Generated: October 30, 2026

Phosgene → HCID 44137272, compound

https://huagongshe.com/reaction/2045829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantHCID 58256489HCID 58256489—
CatalystTolueneHCID 1140—
CatalystPhosgeneHCID 6371—
CatalystTriethylamineHCID 8471—
SolventTolueneHCID 1140—
ProductHCID 44137272HCID 44137272—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(4-fluorophenyl)-1-(2-methyl-2-phenylhydrazinyl)hex-5-en-3-ol (14 mg, 0.04 mmol) and triethylamine (3 drops) was dissolved in toluene (1 mL). The solution was cooled to 0° C. and phosgene (3 drops, 20% toluene solution) was added. After 1 h, more phosgene was added (3 drops, 20% toluene solution) and the reaction was allowed to warm to rt overnight. The solvent was evaporated and the residue was redissolved in toluene. DBU (5 drops) was added and the solution heated to reflux for 4 h. The solvent was evaporated and the residue was purified by preparative HPLC to afford 6-allyl-6-(4-fluorophenyl)-3-(methyl(phenyl)amino)-1,3-oxazinan-2-one (8.8 mg). LC-MS Method 1 m/z=341 (M+1). 1H NMR (CDCl3) δ 7.43-7.37 (br m), 7.25-7.26 (m), 7.19-7.12 (m), 6.99 (t), 6.85 (m), 6.72-6.66 (m), 6.07 (d), 6.73 (m), 5.15-5.05 (m), 3.42 (m), 3.33 (m), 3.14 (s), 2.85 (s), 2.65-2.55 (m), 2.50-2.34 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592409B2
Source datasetuspto-grants-2013_11
ORD IDord-71e2b73ef4554e86877dc9cff5e7361d
Source noteuspto-grants-2013_11