HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → trans-N-(1,2,3,4-tetrahydro-4-methoxy-1-naphthyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N-(4-Oxo-1,2,3,4-tetrahydronaphthalen-1-yl)acetamide | HCID 13037024 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | trans-N-(1,2,3,4-tetrahydro-4-methoxy-1-naphthyl)acetamide | HCID 70617063 | — |
Reaction Steps
A mixture of racemic N-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)acetamide (3.9 g) and 150 ml. tetrahydrofuran (THF) is stirred and 17 ml. of methyl iodide and 24.4 g. of freshly prepared silver oxide are added over a 4-hour period, under a nitrogen atmosphere. After 16 hours, an additional 10 ml. of methyl iodide and 11.4 g. of silver oxide are added over a 4-hour period and stirring is continued for 2 days. The mixture is filtered through a layer of celite and the filter cake washed with THF (2 × 75 ml.). The filtrate and wash solution are combined and evaporated to dryness in vacuo to afford 4.3 g. of solid. The solid is recrystallized from hexane/ether to afford 2.4 g. of title compound, melting point 97°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04089976 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-ee56eb2cb536446aa3b424cafc4775cb |
| Source note | uspto-grants-1978_05 |