HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 10920996, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Valeryl chloride | HCID 61186 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10920996 | HCID 10920996 | 84% |
Reaction Steps
o-Toluidine (55 g) was mixed with 100 ml dry pyridine and 200 ml dry tetrahydrofuran in a 1-L 3-necked round bottom flask fitted with a Trubore stirrer, thermometer and a dropping funnel, under nitrogen. Then, with cooling in a refrigerated bath, valeryl chloride (60.3 g) was added dropwise over 1 hour. The mixture was stirred for another hour at room temperature and then poured onto 500 g ice and water. The precipitate was washed repeatedly with water on a Buchner funnel. The precipitate (88.9 g, 93%) was cyclized according to Verley and Bedure, 1925, Bull. Soc. Chim. Fr. (37): 190 to afford 2-n-butyl indole (67.4 g, 84%) as a very slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06660763B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-b4db60736e814859a8242a2d3dca4082 |
| Source note | uspto-grants-2003_12 |