Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Indan-5-amine | HCID 90496 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Indanyl isocyanate | HCID 5003681 | 203.7% |
Reaction Steps
To a solution of 5-aminoindane (25 g) in anhydrous diethyl ether (1250 ml), under an atmosphere of nitrogen, at 0° C. was added triphosgene (18.3 g). The mixture was stirred at 0° C. for 2 min then triethylamine (64.7 ml) was added until pH8. The mixture was stirred at 0° C. for 10 min then at. 10° C. for 10 min. The undissolved solids were filtered off and the filtrate evaporated in vacuo. The residue was distilled at 100° C./1 mbar to afford the title compound (20 g). 1H NMR (360 MHz, CDCl3) δ2.07 (2H, quin, J=7.5 Hz), 2.86 (4H, m), 6.84 (1H, dd, J=7.9 and 2.0 Hz), 6.94 (1H, s), 7.13 (1H, d, J=7.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05618812 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-8a701233b0aa4b0c8a688b121562a1de |
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| Source note | uspto-grants-1997_04 |
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