HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → HCID 53919156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | HCID 20312395 | HCID 20312395 | — |
| Product | HCID 53919156 | HCID 53919156 | — |
Reaction Steps
A solution of 20.2 g. (0.070 mol.) of N-t-butoxycarbonyl-2-acetoxyglycine n-butyl ester and 8.8 g. (0.075 mol.) of indole in 300 ml. of toluene was slowly distilled over a 30 minutes interval with periodic replacement of the toluene with fresh solvent. After an additional 45 minutes the reaction mixture was cooled and the solvent was evaporated in vacuo. The residue was triturated with hexane to give α-(N-t-butoxycarbonylamino)indole-3-acetic acid n-butyl ester, m.p. 127°-128° (ether-hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03994954 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-8e20fb3c68a94e99a45c6de9dd1c0784 |
| Source note | uspto-grants-1976_11 |