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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986537Generated: October 31, 2026

Tetrahydrofuran → Tert-butyl[4-(3,4-difluoro-benzyl)-5-oxoperhydro-1,4-thiazepin-6-yl]-carbamate

https://huagongshe.com/reaction/1986537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)-1,2-difluorobenzeneHCID 581436—
Reactant(Hexahydro-5-oxo-1,4-thiazepin-6-yl)carbamic acid, (1,1-dimethylethyl) esterHCID 15591256—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl[4-(3,4-difluoro-benzyl)-5-oxoperhydro-1,4-thiazepin-6-yl]-carbamateHCID 5772229161%

Reaction Steps

81 mg of sodium hydride as a 60% suspension in oil (2.03 mmol) are introduced at room temperature into a 50 ml round-bottomed flask, with stirring and under an argon atmosphere, containing 20 ml of THF and 500 mg of 26 (2.03 mmol). The medium is stirred for 1 hour and 420 mg (2.03 mmol) of 3,4-difluorobenzyl bromide are then added. The medium is stirred overnight, 20 ml of EtOAc and 20 ml of water are added to the reaction medium and, after separation of the phases by settling, the organic phase is washed once with 20 ml of water. The organic phase is dried, filtered and then evaporated to dryness. 1.5 g of crude product are recovered, which product is chromatographed on silica (eluent: 80/20 heptane/EtOAc). 460 mg of product 30 are recovered (yield=61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550453B2
Source datasetuspto-grants-2009_06
ORD IDord-eeff02cde84f41ee812a5161a02e1d2b
Source noteuspto-grants-2009_06