HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → HCID 12266980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Ethoxyacetic acid | HCID 12301 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 12266980 | HCID 12266980 | 63% |
Reaction Steps
2-Aminothiophenol was reacted with an equimolar amount of ethoxyacetic acid at 110° C. for 15 hours in a sealed tube. After cooling the reaction mixture, it was neutralized with a 20% aqueous solution of sodium hydroxide, followed by an extraction with ether. Ether was driven off and the residue was then subjected to distillation under reduced pressures, thereby obtaining 2-ethoxymethylbenzothiazole (boiling point: 126°-128° C./4 mmHg; yield: 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04485168 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-77d12fad82044286bf4ed23b261b836a |
| Source note | uspto-grants-1984_11 |