HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986539Generated: October 29, 2026
Dimethylformamide → Tert-butyl[4-(3,5-difluoro-benzyl)-5-oxoperhydro-1,4-thiazepin-6-yl]carbamate
https://huagongshe.com/reaction/1986539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,5-Difluorobenzyl bromide | HCID 518896 | — |
| 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-(3,5-difluoro-benzyl)-5-oxoperhydro-1,4-thiazepin-6-yl]carbamate | HCID 57722274 | 79% |
Reaction Steps
121 mg of sodium hydride as a 60% suspension in oil (3.05 mmol) are introduced at room temperature into a 50 ml round-bottomed flask, with stirring and under an argon atmosphere, containing 20 ml of DMF and 500 mg of 26 (2.03 mmol). The medium is stirred for 1 hour and 454 mg (2.03 mmol) of 3,5-difluorobenzyl bromide are then added. The medium is stirred for 3 hours, 50 ml of EtOAc and 50 ml of water are added to the reaction medium and, after separation of the phases by settling, the organic phase is washed with 50 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 a silica cartridge (20 g, eluent: 80/20 heptane/EtOAc). 600 mg of product 33 are recovered (yield=79%).
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-bc936704ed794c1d9f6b66758f70e013 |
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| Source note | uspto-grants-2009_06 |
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