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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670513Generated: October 27, 2026

Dimethyl Sulfoxide → HCID 59822286, compound

https://huagongshe.com/reaction/1670513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant7-Chloro-3-(2,2,2-trifluoroacetyl)-6-trifluoromethylsulfonyloxy-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 57447747—
ReactantHCID 178418416HCID 178418416—
Catalyst1,3-Bis(diphenylphosphino)propaneHCID 81219—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 59822286HCID 5982228682%

Reaction Conditions

Temperature100 °C

Reaction Steps

Add 7-chloro-3-(2,2,2-trifluoroacetyl)-6-trifluoromethanesulfonyloxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine (213 g, 500 mmol), triethylamine (118 g, 1150 mmol), palladium(II) acetate (5.6 g, 25 mmol) and 1,3-bis(diphenylphosphino)propane (6.4 g, 15 mmol) to anhydrous DMSO (2.1 L) and ethanol (640 mL) in a 1 gallon autoclave. Inert the autoclave with nitrogen then charge the mixture with carbon monoxide at 50 psi and heat at 100° C. for 2 h (monitor reaction by HPLC). Cool the autoclave to room temperature and add the dark reaction mixture to a flask containing water (3.2 L) and EtOAc (3.2 L). Collect the organic layer and back extract the aqueous layer with EtOAc (2.1 L). Wash the combined organic extracts with water (2.1 L). Concentrate the organic layer in vacuo to a dark oil. Purify the crude mixture by chromatography on silica gel eluting with heptane/EtOAc (5:1) to give the desired intermediate as a pale green oil (144 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994163B2
Source datasetuspto-grants-2011_08
ORD IDord-d27d30a1c14e48d98daa99a23ea468d3
Source noteuspto-grants-2011_08