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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784348Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 90961605, compound

https://huagongshe.com/reaction/1784348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantHCID 69063359HCID 69063359—
Catalyst1,3-Bis(diphenylphosphino)propaneHCID 81219—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 90961605HCID 90961605—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of (S)-7-Bromo-2,3,11,11a-tetrahydro-1H,5H-pyrrolo[2,1-c][1,4]-benzoxazepine-5-one (5 g; 17.76 mmol), prepared as described in Example 3J, in dimethylsulfoxide (80 ml) was added palladium acetate (225 mg; 1 mmol), 1,3-bis-(diphenylphosphino)propane (413 mg; 1 mmol), triethylamine (5 ml; 36 mmol) and methanol (4 ml). After stirring under argon until all solids had dissolved the reaction vessel was purged several times with carbon monoxide and placed under an atmosphere of carbon monoxide (balloon). The mixture was then heated to 100° C. and stirred overnight. Further portions of palladium acetate (0.50 mmol) and 1,3-bis-(diphenylphosphino)propane (0.50 mmol) were added and the mixture stirred at 100° C. for a further 6 h. After cooling water (200 ml) was added and the aqueous solution was extracted with three 75 ml portions of ethyl acetate. The combined extracts were dried (Na2SO4) and solvent evaporated under reduced pressure. The resulting brown oil was purified by column chromatography eluting with ethyl acetate. Further purification by recrystallisation from diethyl ether gave methyl (S)-2,3,11,11a-tetrahydro-1H,5H-pyrrolo[2,1-c][1,4]benzoxazepine-5-one-7-carboxylate (3.13 g) as a white crystalline solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504390B2
Source datasetuspto-grants-2009_03
ORD IDord-c8dbc932f36e4d468cc1d5184fcf87ba
Source noteuspto-grants-2009_03