HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1660367Erstellt: 23. Oktober 2026
Triethanolamine → 1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]
https://huagongshe.com/de/reaction/1660367
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethanolamine | HCID 7618 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | 1-(2-Aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochloride | HCID 12801598 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine] | HCID 12801608 | — |
Reaktionsschritte
A slurry of 10.36 g of 1-(2-aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochloride of Example 1b in 60 ml of chloroform is treated portionwise with 12.3 ml of triethanolamine. The resulting mixture is cooled in an ice bath and treated dropwise over 40 minutes with a solution of 2.7 ml of ethyl chloroformate in 20 ml of chloroform. After stirring at room temperature for 1 hour, an additional 3.0 ml of ethyl chloroformate is added and the mixture is permitted to stand 16 hours. The product is washed thrice with water, brine, dried over anhydrous sodium sulfate, concentrated and pumped on under high vacuum to give a crude carbamate. Chromatography on silica gel (100 g) using ether-methylene chloride affords an oil. The material crystallizes on prolonged standing to yield 1-[2-(ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine], mp 99.5°-101.0° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04307235 |
|---|
| Quelldatensatz | uspto-grants-1981_12 |
|---|
| ORD ID | ord-32ed2725ab6a472288674baea068fbd2 |
|---|
| Quellennotiz | uspto-grants-1981_12 |
|---|