HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467995Generated: October 31, 2026
Triethylamine → ethyl 1H-indol-5-ylcarbamate
https://huagongshe.com/reaction/1467995
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 5-Aminoindole | HCID 78867 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 1H-indol-5-ylcarbamate | HCID 54033885 | 35.2% |
Reaction Steps
To a stirred solution of 1H-indol-5-amine (11 g, 83.2 mmol) and triethyl amine (25.22 g, 250 mmol) in dichloromethane (110 mL) at −10° C., ethyl-chloro-formate (13.5 g 124.8 mmol) was added dropwise and stirred at 0° C. for 2-3 h. The reaction was quenched with water and the mixture was extracted with ethyl acetate. The organic layer was concentrated in vacuo and the resultant residue was purified by flash column chromatography to give ethyl-1H-indol-5-ylcarbamate (5.980 g, 35.2%); MS: 205 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000175B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-7af1d86742654a98bab712e45762843f |
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| Source note | uspto-grants-2015_04 |
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