HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649937Generated: October 31, 2026
Benzoic Acid → 5-Benzoylamino-1-hydroxy-5,6,7,8-tetrahydro-naphthalene
https://huagongshe.com/reaction/1649937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 5-Amino-1-hydroxy-5,6,7,8-tetrahydro-naphthalene hydrobromide | HCID 19855451 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Benzoylamino-1-hydroxy-5,6,7,8-tetrahydro-naphthalene | HCID 14014955 | — |
Reaction Steps
50 mmol of benzoic acid and 50 mmol of 1-hydroxybenzotriazole (HOBT) are taken in 200 ml of absolute tetrahydrofuran at 0° C. 55 mmol of dicyclohexylcarbodiimide (DCC) are added under N2 and the mixture is stirred at 0° C. for 1 hour and then at room temperature for 1 hour. 50 mmol of 5-amino-1-hydroxy-5,6,7,8-tetrahydro-naphthalene hydrobromide and 50 mmol of triethylamine are added to this solution and the mixture is stirred at room temperature for 6 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921998 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-f0a606568b2940ae8319a328946e32b7 |
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| Source note | uspto-grants-1990_05 |
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