HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfide → 1,3-Dihydro-2-benzothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | 1-(Dibromomethyl)-2-methylbenzene | HCID 639040 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,3-Dihydro-2-benzothiophene | HCID 137608 | — |
Reaction Steps
The compounds of formula 4 where n is 0, 1 or 2 are prepared by a modification of the procedure of ##STR13## Oliver, et al., in Chem. and Ind., 1024 (1965). α,α-Dibromo-o-xylene is reacted with sodium sulfide in ethanol to form 1,3-dihydrobenzo[c]thiophene. The thiophene compound is oxidized to the corresponding dioxide by means of hydrogen peroxide, m-chloroperzenxoic acid or other suitable oxidants or to the monoxide (Can. J. Chem., 51, 4082 (1973) using sodium metaperoidate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04219648 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-6c9b7de8507a44769bea48a9d8192380 |
| Source note | uspto-grants-1980_08 |