HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36934Generated: October 28, 2026
tert-Butanol → 3-tert-butyloxycarbonylamino-4-(2-methylphenyl)-7,8-dihydro-6H-cyclopenta[g][1]benzopyran-2-one
https://huagongshe.com/reaction/36934
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 4-(2-Methylphenyl)-2-oxo-2,6,7,8-tetrahydrocyclopenta[g][1]benzopyran-3-carboxylic acid | HCID 10358630 | — |
| Product | 3-tert-butyloxycarbonylamino-4-(2-methylphenyl)-7,8-dihydro-6H-cyclopenta[g][1]benzopyran-2-one | HCID 19782166 | — |
Reaction Steps
To a solution of 4-(2-methylphenyl)-2-oxo-2,6,7,8tetrahydrocyclopenta [g][1]benzopyran-3-carboxylic acid (2.5 g) and diphenyl phosphoryl azide (DPPA, 2.58 g) in tert-butanol (25 ml) was added triethylamine (1.1 ml) dropwise and the mixture was stirred at room temperature for 30 minutes and, then, refluxed for 4 hours. The solvent was distilled off and the residue was diluted with water and extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and distilled to remove the solvent, whereby 3-tert-butyloxycarbonylamino-4-(2-methylphenyl)-7,8-dihydro-6H-cyclopenta[g] [1]benzopyran-2-one was obtained as oil. The oil was crystallized from hexane (2.95 g, 96.7%). Recrystallization from ethanol-hexane gave colorless prisms, m.p. 154°-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05418239 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-717fbb7035884a4bac0037e5a542223b |
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| Source note | uspto-grants-1995_05 |
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