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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Bromomethyl)-1,2-difluorobenzene | HCID 581436 | — |
| Reactant | (Hexahydro-5-oxo-1,4-thiazepin-6-yl)carbamic acid, (1,1-dimethylethyl) ester | HCID 15591256 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl[4-(3,4-difluoro-benzyl)-5-oxoperhydro-1,4-thiazepin-6-yl]-carbamate | HCID 57722291 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550453B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-eeff02cde84f41ee812a5161a02e1d2b |
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| Source note | uspto-grants-2009_06 |
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