HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 12799916, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 20431900 | HCID 20431900 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 12799916 | HCID 12799916 | 36% |
Reaction Steps
A mixture of [4-methoxycarbonyl-2-(n-dodecanamido)benzyl]triphenylphosphonium bromide (23.8 g) and potassium tert.-butoxide (3.9 g) were added to dry toluene (680 ml). The stirred mixture was heated to reflux for 15 minutes and cooled to room temperature. Ethyl acetate (1.5 liter) and saturated brine (750 ml) were added; the mixture was shaken and the organic phase separated. The organic extract was dried over magnesium sulphate and was evaporated in vacuo to give an oil. The oil was purified by chromatography on a silica column using chloroform as eluant to give a crude solid which was recrystallised from methanol to give methyl 2-(n-undecyl)indole-6-carboxylate (4.1 g) as an off-white solid, m.p. 83°-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04493843 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-6578a46a732743d4b008eec2aa24ab1b |
| Source note | uspto-grants-1985_01 |