HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443257Generated: October 31, 2026
Dimethyl Sulfate → HCID 21193434, compound
https://huagongshe.com/reaction/443257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | HCID 21193301 | HCID 21193301 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21193434 | HCID 21193434 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891889 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-a12e3155e0a44783a06c7d3d32228bf6 |
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| Source note | uspto-grants-1999_04 |
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