HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl chloride → HCID 15860210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | HCID 15907399 | HCID 15907399 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 15860210 | HCID 15860210 | 65% |
Reaction Steps
To a stirred solution of N-(3-cyclopentyloxy-4-methoxyphenylacetyl)-2-hydroxy-5-chloroaniline (78g, 0.21 mol) in ethanol (600 ml) and 1N NaOH in methanol (213 ml) was added allyl chloride (23.3 g, 0.31 mol). The mixture was heated under reflux for 8 hours, after which it was diluted with water and extracted twice with ethyl acetate. Evaporation of the ethyl acetate and crystallization of the residue from methanol gave 56.4 g (65%) of the title compound, mp 75°-76.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665737 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-560437e398eb426d8aa6f33a2e27fa52 |
| Source note | uspto-grants-1997_09 |