HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965215Generated: November 1, 2026
p-Toluenesulfonic acid → (+/-) trans 1-(3,4-Dichloroanilino)-2-ethoxycarbonylaminoindane
https://huagongshe.com/reaction/965215
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-Dichloroaniline | HCID 7257 | — |
| Reactant | (3AR,8bS)-2-ethoxy-4,8b-dihydro-3aH-indeno[2,1-d]oxazole | HCID 18661302 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (+/-) trans 1-(3,4-Dichloroanilino)-2-ethoxycarbonylaminoindane | HCID 53724852 | 72.8% |
Reaction Steps
A solution of (±) cis-2-ethoxy-3a,8b-dihydro-4H-indeno[2,1-d]oxazole (1.0 g, 0.005 mol) in dry toluene (20 ml) was treated with 3,4-dichloroaniline (0.81 g, 0.005 mol) and a catalytic amount of p-toluenesulfonic acid (5 ml of an anhydrous 0.1M solution of p-toluenesulfonic acid in benzene). The mixture was heated under nitrogen at 60° C. for 3 h. The reaction was worked up as described in Preparation 5. Purification on a silica gel column using 1% ethanol in chloroform as eluant afforded the title compound as a solid (1.33 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773463 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-845aecd90193438a9509dd5805eb6fa5 |
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| Source note | uspto-grants-1998_06 |
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