HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 3-Methyl-6-(2-bromoethyl)benzothiazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 3-Methyl-6-(bromoacetyl)benzothiazolinone | HCID 86746657 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 3-Methyl-6-(2-bromoethyl)benzothiazolinone | HCID 70183836 | — |
Reaction Steps
In a 500-cm3 ground-necked flask surmounted by a condenser and placed in an oil bath, 42.9 g (0. 15 mol) of 3-methyl-6-(bromoacetyl)benzothiazolinone are dissolved in 77 cm3 of trifluoroacetic acid with magnetic stirring and while the temperature is stabilized at 60° C. 52.7 cm3 (0.33 mol) of triethylsilane are introduced dropwise via a dropping funnel. After the addition, the heating is stopped and the mixture is left stirring vigorously for 30 hours. The reaction medium is hydrolyzed by pouring it into ice-cold water, and the precipitate obtained is drained and washed with water until the filtrate is neutral and then with hexane. The product is dried and recrystallized in cyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05268381 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-0a6683e7e9db47c689a4d9fb53bb1bb7 |
| Source note | uspto-grants-1993_12 |