HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Alimadol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21534186 | HCID 21534186 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Alimadol | HCID 176882 | 93% |
Reaction Steps
16.7 g. of N-(3,3-diphenyl-3-methoxypropyl)-trifluoroacetamide, prepared according to Example 4, and 24.2 g. of allyl bromide in 150 ml. of anhydrous acetone are heated to 50°C. and 11.2 g. of powdered potassium hydroxide are added. The mixture is then boiled for 5 minutes and the solvent is distilled off in vacuo. The residue is boiled for one hour with 100 ml. of water and 100 ml. of methanol and is worked up as in Example 4. 13.1 g. of 1,1-diphenyl-1-methoxy-3-allylaminopropane of melting point 45° to 50°C. are obtained, corresponding to a yield of 93% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03960960 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-60efb1f5ec024113a75fdb0fceebe1bb |
| Source note | uspto-grants-1976_06 |