HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904906Generated: October 30, 2026
Dimethyl Sulfate → HCID 13565195, compound
https://huagongshe.com/reaction/904906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13565194 | HCID 13565194 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13565195 | HCID 13565195 | — |
Reaction Steps
A mixture of α-(N-isobutylamino)-3-phenoxybenzeneacetonitrile (28.0 g; 0.1 mole), dimethyl sulfate (12.6 g; 0.1 mole), anhydrous potassium carbonate (15.0 g) and anhydrous acetone (100 ml) was stirred at a temperature of 50° C. for a period of 16 hours. The mixture was filtered and the solvent was removed from the filtrate by distillation under reduced pressure. The residue was treated with anhydrous diethyl ether, the etherial solution was separated and the ether was evaporated to give α-(N-isobutyl-N-methylamino)-3-phenoxybenzeneacetonitrile as a yellow oil. Proton nuclear magnetic resonance spectrum (d6 -acetone; δ in ppm): 0.85 (6H, d of d); 1.83 (1H, m); 2.23 (3H, s); 5.19 (1H, s); 7.0-7.5 (9H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04420614 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-97e697c9df584afbb4498d015be1ea69 |
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| Source note | uspto-grants-1983_12 |
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