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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986543Generated: November 1, 2026

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

https://huagongshe.com/reaction/1986543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-butoxybenzeneHCID 12785266—
Reactant(Hexahydro-5-oxo-1,4-thiazepin-6-yl)carbamic acid, (1,1-dimethylethyl) esterHCID 15591256—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl[4-(4-butoxybenzyl)-5-oxoperhydro-1,4-thiazepin-6-yl]carbamateHCID 57722320156.7%

Reaction Steps

81 mg of sodium hydride as a 60% suspension in oil (2.03 mmol) are introduced at room temperature into a 25 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 1.1 g (2.34 mmol) of 4-butoxybenzyl bromide are then added. The medium is stirred for 16 hours, 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 with 10 ml of water. The organic phase is dried, filtered and then evaporated to dryness to give 1.3 g of crude product, which product is chromatographed on a silica cartridge (25 g) with a 90/10 heptane/EtOAc mixture. 420 mg of product 39 are recovered (yield=53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550453B2
Source datasetuspto-grants-2009_06
ORD IDord-5aa79f004d4d4cc7a136726e0e2de470
Source noteuspto-grants-2009_06