HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-methylsulfanyl-1H-indole → Indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-methylsulfanyl-1H-indole | HCID 10888252 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | Indole | HCID 798 | — |
Reaction Steps
conversion of the dimethyl acetal from part A to 3-methylthioindole was accomplished by stirring 0.50 g (2.20 mmol) of the dimethylacetal dissolved in 25 ml of ethyl ether for 2 hr. with 10 ml of 0.5 N aqueous hydrogen chloride. The ethereal layer was separated, treated with a saturated sodium bicarbonate solution, dried, filtered and evaporated to yield 0.35 g (2.14 mmol, 97%) of the oily 3-methylthioindole. This 3-methylthioindole was treated with Raney nickel as described to form indole, identified by comparison with an authentic sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101583 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-1879321d2c434b6f9e34acaa698ee7e2 |
| Source note | uspto-grants-1978_07 |