HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-(4-Methylcyclohexoxy)ethylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 14473322 | HCID 14473322 | — |
| Product | 2-(4-Methylcyclohexoxy)ethylacetate | HCID 131714148 | — |
Reaction Steps
5.65 Grams (0.04 moles) of 2-(4-methylcyclohexoxy)ethanol (prepared above), 0.8 gm of Amberlyst 15 and 100 ml. of acetic anhydride are charged to a 250 ml flask fitted with a magnetic stirrer and Friedrick condenser. The mixture is heated at reflux for 11/2hours, filtered, and acetic anhydride removed by evaporation. The mixture is distilled and 7.92 gms of 2-(4-methylcyclohexoxy)ethylacetate obtained. The structure of the 2-(4-methylcyclohexoxy)ethylacetate is confirmed by NMR. The 2-(4-methylcyclohexoxy)ethylacetate has an extremely pleasant natural, fruity, wine-like odor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04504412 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-16a387c22b5a4d809ce39d4cfbe3519c |
| Source note | uspto-grants-1985_03 |