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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443257Generated: October 31, 2026

Dimethyl Sulfate → HCID 21193434, compound

https://huagongshe.com/reaction/443257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium hydrideHCID 82127—
ReactantHCID 21193301HCID 21193301—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21193434HCID 21193434—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of potassium hydride (0.40 g, dry weight, 10 mmol; obtained from washing 0.97 g of 35% potassium hydride dispersion in mineral oil with hexanes and drying under a stream of argon) in anhydrous THF (45 mL), N-tert-butoxycarbonyl-4-(3-methylbenzyl)-4-hydroxymethylpiperidine (1.89 g, 5.9 mmol) in THF (15 mL) was added. The resultant mixture was stirred at room temp. for 1 h, and treated with dimethyl sulfate (1.13 mL, 11.9 mmol). The reacting mixture was stirred at room temp. overnight. The product mixture was cooled to 0° C., quenched with water, and diluted with ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 10% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-a12e3155e0a44783a06c7d3d32228bf6
Source noteuspto-grants-1999_04