HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279651Generated: November 2, 2026
Toluene → 1-Benzyl-4-[3-(tert-butoxycarbonylamino)-1-fluorocyclobutan-3-yl]-2-pyrrolidone
https://huagongshe.com/reaction/1279651
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Benzyl-4-[3-(tert-butoxycarbonylamino)-1-hydroxycyclobutan-3-yl]-2-pyrrolidone | HCID 18427824 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzyl-4-[3-(tert-butoxycarbonylamino)-1-fluorocyclobutan-3-yl]-2-pyrrolidone | HCID 18427800 | 30% |
Reaction Steps
A 1.79 g (4.96 mmol) portion of 1-benzyl-4-[3-(tert-butoxycarbonylamino)-1-hydroxycyclobutan-3-yl]-2-pyrrolidone (Isomer B1) was dissolved in a mixed solvent consisting of 50 ml of toluene and 20 ml of dichloromethane to which, while cooling in an ice bath with stirring, was then added 1.31 ml (9.92 mmol) of diethylaminosulfur trifluoride, subsequently carrying out 12 hours of stirring at room temperature. While cooling in an ice bath with stirring, the reaction solution was alkalified by slowly adding saturated sodium bicarbonate aqueous solution and then mixed with chloroform to carry out separation of layers, and the resulting organic layer was washed with saturated brine. The aqueous layer was again extracted with chloroform, and the organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under a reduced pressure and the resulting residue was purified by a silica gel column chromatography to give 541 mg (30.0%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448266B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-134ab0e49ef24bd9b17c42f88ff872dc |
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| Source note | uspto-grants-2002_09 |
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