HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 2-(7-hydroxynaphth-1-yl)ethanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 18007940 | HCID 18007940 | — |
| Product | Methyl 2-(7-hydroxynaphth-1-yl)ethanoate | HCID 18007925 | — |
Reaction Steps
Dissolve the compound obtained in Step A in 100 ml of methanol. Cool the mixture in an ice-bath. Add thionyl chloride dropwise and maintain the reaction mixture at that temperature for 20 minutes after the addition. Leave for 1 hour at room temperature with stirring. Remove the methanol by evaporation under reduced pressure, and recrystallise the resulting solid from a mixture of toluene/cyclohexane (4/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06319930B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-45a15b665ca14d69b46df7eb85c8eabe |
| Source note | uspto-grants-2001_11 |