HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20477976, compound → 2-Aminothiophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20477976 | HCID 20477976 | — |
| Reactant | HCID 20496113 | HCID 20496113 | — |
| Product | 2-Aminothiophenol | HCID 8713 | — |
| Product | 2,3-Epoxy-2,3-dimethylbutane | HCID 21159 | — |
Reaction Steps
Analogously to Example 1, the required 2,2,3,3-tetramethyl-2,3-dihydro-4H-1,4-benzothiazine is obtained as a colourless oil having a boiling point of 89° C./0.04 mbar using 2-(2-hydroxy-1,1,2-trimethylpropylthio)-aniline, melting point of from 60° to 62° C., boiling point of 125° C./0.1 mbar (obtained from tetramethyloxirane and 2-aminothiophenol). nD20 =1.5955; the mass spectrum shows a molecular ion at 207 (74% relative intensity) and as main fragments 192 (24%), 177 (14%), 164 (100%), 150 (44%), 132 (70%), 125 (24%), 109 (15%), 92 (22%), 42 (17%) and 41 (16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04393206 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-c750c92c8c4143229a62b3bf09f86205 |
| Source note | uspto-grants-1983_07 |