HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 10616100, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 178515054 | HCID 178515054 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10616100 | HCID 10616100 | — |
Reaction Steps
To a solution of sodium ethoxide in ethanol (20 ml) (prepared from 0.46 g sodium) was added 3-(5-tetrazolyl) thioxanthone-10,10-dioxide (6.24g). Methyl iodide (2.84 g) was added and the mixture boiled under reflux for 2 hrs. During the reflux period a yellow product was deposited. On cooling it was filtered off, washed with water and recrystallised twice from acetic acid to give 3-(2-methyl-5-tetrazolyl)thioxanthone-10,10-dioxide as yellow needles, m.p. 204°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04103015 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-62b3e132b37e4e1387e1affdba498afd |
| Source note | uspto-grants-1978_07 |