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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760011Generated: November 1, 2026

Chlorotrimethylsilane → HCID 86591873, compound

https://huagongshe.com/reaction/1760011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86591872HCID 86591872—
SolventTriethylamineHCID 8471—
ProductHCID 86591873HCID 86591873—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 3.2 ml of tetrahydrofuran were added 0.37 g of 4-chloro-6-(cis-2-hydroxycyclohexyloxy)pyrimidine and 0.45 ml of triethylamine, to which 0.25 ml of chlorotrimethylsilane was slowly added dropwise with stirring at 0° C. After stirring at room temperature for 3 hours, the reaction mixture was then poured into a saturated aqueous ammonium chloride solution and extracted three times with ethyl acetate. The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.5 g of 4-chloro-6-(cis-2-trimethylsilanyloxycyclohexyloxy)pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838463B2
Source datasetuspto-grants-2005_01
ORD IDord-38bb0423c94c447391980a70613ccfba
Source noteuspto-grants-2005_01