HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473094Generated: October 26, 2026
Diethyl Ether → benzyl N-(5-bromo-2,3-dihydro-1H-inden-1-yl)carbamate
https://huagongshe.com/reaction/473094
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-bromo-2,3-dihydro-1H-inden-1-amine | HCID 22228388 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | benzyl N-(5-bromo-2,3-dihydro-1H-inden-1-yl)carbamate | HCID 67088086 | 82.4% |
Reaction Steps
To a vigorously stirred solution of 5-bromo-2,3-dihydro-1H-inden-1-amine (8.54 g, 40.3 mmol) and potassium carbonate (11.1 g, 80 mmol) in water (100 mL) and ethyl acetate (100 mL) was added benzyl chloroformate (7.56 g, 44.3 mmol). The reaction was stirred at rt overnight before being diluted with water (200 mL) and dichloromethane (200 mL). The organic phase was collected and the aqueous phase was extracted once more with dichloromethane (100 mL). The clear colourless organic layers were dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford a white solid. The material was co-evaporated once with diethyl ether and the residue was triturated with diethyl ether. The white solid was collected by filtration and dried on air to afford the title compound as a white solid (11.5 g, 82%). MS (ESI): m/z [M+H]+ 347.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633237B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-4acdf977ef684dc1841282fcb0655c48 |
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| Source note | uspto-grants-2014_01 |
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