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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014088Generated: October 31, 2026

Triethylamine → F15845

https://huagongshe.com/reaction/1014088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 11788638HCID 11788638—
ReactantHCID 86637446HCID 86637446—
SolventTolueneHCID 1140—
ProductF15845HCID 11566989—

Reaction Conditions

Temperature105 °C

Reaction Steps

6.5 g (35.9 mmol) of (R)-3,4-dihydro-2H-1,5-benzoxathiepin-3-amine and 11 g (30 mmol) of (S)-3-(2-methoxyphenyl-sulfanyl)-2-methylpropyl 4-methylbenzenesulfonate in 33 ml of toluene are introduced into a three-necked flask under an inert atmosphere. 6 g (60 mmol) of triethylamine are added and then the reaction mixture is heated with stirring at 105° C. for 24 hours. After returning to ambient temperature, 33 ml of toluene are added. The organic phase is washed twice with 66 ml of demineralised water and is then decolourised by stirring for one hour in the presence of 2 g of Black CXV. After concentrating under reduced pressure, driving-off with 33 ml of ethanol 100 is carried out. The title product is obtained in the form of a yellow oil (8.85 g; 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982054B2
Source datasetuspto-grants-2011_07
ORD IDord-1b571ddc9f244bbdb4378baa7eeba692
Source noteuspto-grants-2011_07