HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927199Generated: October 31, 2026
2-Methyltetrahydrofuran → HCID 131735049, compound
https://huagongshe.com/reaction/927199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-[3-(Trifluoromethyl)anilino]cyclopent-2-en-1-one | HCID 90311057 | — |
| Reactant | Tert-butyl ((2-bromo-4-cyanophenyl)(phenylsulfonyl)methyl)carbamate | HCID 131735048 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131735049 | HCID 131735049 | — |
Reaction Steps
Sodium hydride (60% in mineral oil, 360 mg, 9.00 mmol) is added in portions to a mixture of 3-(3-(trifluoromethyl)phenylamino)cyclopent-2-enone (2.16 g, 8.96 mmol) and 2-methyltetrahydrofuran (30 mL). After 30 min tert-butyl (2-bromo-4-cyanophenyl)(phenyl-sulfonyl)methylcarbamate (Step 1, 3.35 g, 7.43 mmol) is added and the mixture is stirred at room temperature for 2 h. Water is added and the phases are separated. The aqueous phase is extracted twice with ethyl acetate, and the combined organic phases are washed with water, dried over MgSO4 and concentrated under reduced pressure. The residue is treated with tert-butyl methyl ether, and the mixture is stirred for 15 min. The precipitate is filtered, washed with tert-butyl methyl ether, and dried. Yield: 3.18 g. ESI mass spectrum: [(79Br)-M+H]+=550, [(81Br)-M+H]+=552; Retention time HPLC: 0.73 min (X012_S01).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09290459B1 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-5d00eab3aed94e938655f07e14c055c6 |
|---|
| Source note | uspto-grants-2016_03 |
|---|