HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235198Generated: November 1, 2026
Benzyl Alcohol → (1-Phenyl-cyclohexyl)-carbamic acid benzyl ester
https://huagongshe.com/reaction/2235198
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Phenylcyclohexane-1-carboxylic acid | HCID 70817 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (1-Phenyl-cyclohexyl)-carbamic acid benzyl ester | HCID 59299316 | 38% |
Reaction Steps
Dissolve 1-phenyl-cyclohexanecarboxylic acid (5.0 g, 24.48 mmol) in benzene (200 mL). Add triethylamine (2.45 g, 24.48 mmol), diphenylphosphoryl azide (6.74 g, 24.48 mmol), and benzyl alcohol (3.97 g, 36.72 mmol) under nitrogen. Stir and heat the reaction mixture to 80° C. Continue to heat the reaction at 80° C. for 8 hours, then cool to room temperature. Add water (250 mL), and extract the aqueous layer with ethyl acetate (3×300 mL). Combine the organic layers and dry with Na2SO4, filter, concentrate and purify by flash column chromatography (silica gel, 5-25% of EtOAc/Hexane) to give 2.87 g (38%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713979B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-2fbe188cdd314f84b899a53aec685cf6 |
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| Source note | uspto-grants-2010_05 |
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