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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927199Generated: October 31, 2026

2-Methyltetrahydrofuran → HCID 131735049, compound

https://huagongshe.com/reaction/927199

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantSodium hydrideHCID 24758—
Reactant3-[3-(Trifluoromethyl)anilino]cyclopent-2-en-1-oneHCID 90311057—
ReactantTert-butyl ((2-bromo-4-cyanophenyl)(phenylsulfonyl)methyl)carbamateHCID 131735048—
SolventWaterHCID 962—
ProductHCID 131735049HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290459B1
Source datasetuspto-grants-2016_03
ORD IDord-5d00eab3aed94e938655f07e14c055c6
Source noteuspto-grants-2016_03