HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzenethiol → (+/-)-1-(((2-Bromophenyl)thio)methyl)-1-ethylpentanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzenethiol | HCID 80598 | — |
| Reactant | 2-Butyl-2-ethylaziridine | HCID 21709970 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (+/-)-1-(((2-Bromophenyl)thio)methyl)-1-ethylpentanamine | HCID 18968814 | 113.4% |
Reaction Steps
To a solution of 2-bromothiophenol (13.5 g, Lancaster) in methanol (45 ml) was added dropwise 2-butyl-2-ethylaziridine (10.0 g, Synthetic Example 1(f)). The mixture was stirred at room temperature for 1 hour. Solvent was evaporated to afford the title product as a light yellow oil (25.6 g). 1H NMR consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05817652 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-54b6725a54c643498ef18e10b19f3721 |
| Source note | uspto-grants-1998_10 |