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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037442Generated: November 1, 2026

Triethylamine → HCID 58109414, compound

https://huagongshe.com/reaction/2037442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
Reactant(R)-6-allyl-3-((S)-1-(4-bromophenyl)ethyl)-6-(4-fluorophenyl)-1,3-oxazinan-2-oneHCID 53473487—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
ProductHCID 58109414HCID 58109414164.7%

Reaction Steps

To a 16 mm culture tube with a Teflon-coated stirring bar, a solution of (R)-6-allyl-3-((S)-1-(4-bromophenyl)ethyl)-6-(4-fluorophenyl)-1,3-oxazinan-2-one (87 mg, 0.209 mmol) in dry DMSO (4 mL) and dry methanol (1.5 mL), triethylamine (60 μL, 2 equiv), Pd(OAc)2 (10 mg, 0.2 equiv) and 1,3-bis(diphenylphosphino)propane (35 mg, 0.4 equiv) were added. The tube was sealed with a septum and Parafilm tape. The reaction mixture was purged with CO gas through a long needle for 1 min. A balloon filled with CO gas was attached to maintain a CO atmosphere. The reaction mixture was submerged in an oil bath preheated to 85° C. and stirred vigorously. After 12 h, LC-MS showed the reaction was complete. The mixture was filtered through a thin pad of Celite. The Celite was washed with EtOAc (35 mL). The filtrate was washed with 3% aq HCl (10 mL), water (2×8 mL) and brine (2×7 mL), and dried over Na2SO4. After filtration and concentration, the residue was purified by chromatography on a 12-g silica gel cartridge eluted with a 10-60% EtOAc in hexanes gradient to afford methyl 4-((S)-1-((R)-6-allyl-6-(4-fluorophenyl)-2-oxo-1,3-oxazinan-3-yl)ethyl)benzoate (68.4 mg, 83%). LC-MS Method 1, tR=1.79 min, m/z=398. 1H NMR (CDCl3) 7.79 (d, 2H), 7.26 (m, 2H), 7.04 (t, 2H), 6.94 (d, 2H), 5.69 (m, m, 2H), 5.07 (dd, 2H), 3.89 (s, 3H), 2.94 (m, 1H), 2.58 (m, 2H), 1.54 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-6719f8550aed4ee08af1a16af0c3a258
Source noteuspto-grants-2013_11