HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 13093615, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Butyl 7-hydroxy-1H-indole-2-carboxylate | HCID 13093609 | — |
| Reactant | HCID 13416931 | HCID 13416931 | — |
| Product | HCID 13093615 | HCID 13093615 | — |
Reaction Steps
Under ice cooling and agitation, 818 mg of tert-butylaminoacetonitrile hydrochloride and 1.2 g of 7-hydroxyindole-2-carboxylic acid n-butyl ester are added to a solution of 2.7 g of aluminum chloride in 20 ml of nitrobenzene. Then gaseous hydrogen chloride is introduced into the mixture at 0° to 3° C. for 7 hours, the reaction mixture is stirred for 16 hours at 0°-3° C., and then poured into ice water. The mixture is agitated for 10 minutes and then the precipitate is vacuum-filtered. The precipitate is recrystallized from isopropanol, thus obtaining 765 mg of 4-tert-butylaminoacetyl-7-hydroxyindole-2-carboxylic acid n-butyl ester hydrochloride, decomposition point 203°-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04835175 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-fd4aac5143a94cd3a4d6ac8afb264683 |
| Source note | uspto-grants-1989_05 |