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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243192Generated: October 30, 2026

Sodium hydride → HCID 68508421, compound

https://huagongshe.com/reaction/2243192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86608971HCID 86608971—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68508421HCID 68508421—

Reaction Steps

To a stirring solution comprised of a mixture of methanesulfonic acid 3-sec-butylcarbamoyl-3-(4-cyano-3-trifluoromethyl-phenoxy)-2,2-dimethyl-propyl ester diastereomers (1.89 g; 4.2 mmol) in tetrahydrofuran (10 mL) at ambient temperature under a nitrogen atmosphere is added a 60% sodium hydride mineral oil dispersion (0.34 g; 8.4 mmol) in portions. The reaction mixture is stirred overnight. The reaction mixture is carefully neutralized with saturated aqueous ammonium chloride and is extracted with ethyl acetate. The organic phase is washed with a brine solution and is dried over anhydrous magnesium sulfate. The organic solution is concentrated in vacuo to afford 1.47 g of a viscous residue comprised of two diastereomers; HPLC UV purity: 92% (two diastereomers.) The diastereomers are separated by flash silica column chromatography (Biotage Horizon chromatography system; 100 g of silica gel, Biotage 40+M silica cartridge.) Elution with a gradient (100% hexanes to 30% ethyl acetate over 3204 mL) will afford complete separation of the diastereomers:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674819B2
Source datasetuspto-grants-2010_03
ORD IDord-4a1238812a4945f5837ecfa1e3e4f835
Source noteuspto-grants-2010_03