HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555672Generated: October 30, 2026
Benzyl Alcohol → Methyl 4-{[(benzyloxy)carbonyl]amino}bicyclo[2.2.2]octane-1-carboxylate
https://huagongshe.com/reaction/555672
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 4-(Methoxycarbonyl)bicyclo[2.2.2]octane-1-carboxylic acid | HCID 11042062 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4-{[(benzyloxy)carbonyl]amino}bicyclo[2.2.2]octane-1-carboxylate | HCID 23149677 | — |
Reaction Steps
Methyl hydrogen bicyclo[2.2.2]octane-1,4-dicarboxylate (25.0 g), diphenylphosphoryl azide (32.5 g), triethylamine (17.3 mL) and toluene (500 mL) were mixed together. The mixture was stirred for 2 hours at room temperature and was heated and refluxed for 2 hours. To the resulting mixture, benzylalcohol (122 mL) was added and the mixture was further heated and refluxed for 17 hours. Subsequently, the mixture was allowed to cool and was sequentially washed with a 10% aqueous citric acid, saturated aqueous solution of sodium bicarbonate, and saturated brine. The mixture was then dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluant:hexane:ethyl acetate=2:1) to give methyl 4-benzyloxycarbonylaminobicyclo[2.2.2]octane-1-carboxylate (32.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053465B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-c67f13f27e83494e9b7a0ba468efce74 |
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| Source note | uspto-grants-2011_11 |
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