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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250375Generated: October 30, 2026

Ammonium Chloride → HCID 69944199, compound

https://huagongshe.com/reaction/1250375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(Chloromethyl)dimethylisopropoxysilaneHCID 266137—
ReactantMagnesiumHCID 5462224—
ReactantHCID 69943808HCID 69943808—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69944199HCID 69944199—
ProductHCID 178460657HCID 178460657—

Reaction Steps

(Dimethylisopropoxysilyl)methylmagnesium chloride was prepared from a solution of 5.74 g (34.4 mmol) of chloromethyldimethylisopropoxysilane in 40 ml tetrahydrofuran and 0.84 g (34.4 mmol) of metallic magnesium. A solution of 4.65 g (17.2 mmol) of (2R)-2′,3′-difluoro-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)propiophenone [prepared as described in Step 7(i) above] in 20 ml of tetrahydrofuran was added to the solution of the Grignard reagent at 0° C. with stirring. The resulting mixture was stirred at ambient temperature for 30 minutes, after which the reaction was stopped by the addition of a saturated aqueous ammonium chloride solution to the reaction mixture. The reaction product was extracted with ethyl acetate. The organic layer was washed with aqueous sodium chloride solution and concentrated to afford 8.1 g of crude (2S,3R)-2-(2,3-difluorophenyl)-1-(isopropoxydimethylsilyl)-3-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)-2-butanol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337403B1
Source datasetuspto-grants-2002_01
ORD IDord-e648efe6eabd4489960bb10fc1ea0cb7
Source noteuspto-grants-2002_01