HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370295Generated: November 1, 2026
Benzyl Alcohol → [8-(4-Fluoro-phenyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-carbamic acid benzyl ester
https://huagongshe.com/reaction/2370295
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 | 1,4-Dioxaspiro[4.5]decane-8-carboxylic acid, 8-(4-fluorophenyl)- | HCID 12230246 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [8-(4-Fluoro-phenyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-carbamic acid benzyl ester | HCID 59226068 | — |
Reaction Steps
3 g of 8-(4-Fluoro-phenyl)-1,4-dioxa-spiro[4.5]decane-8-carboxylic acid (75) and 3.3 mL of triethyl amine were dissolved in 50 mL of dry toluene. At 0° C. 2.83 mL of diphenyl phosphoryl azide was added dropwise. The mixture was stirred at room temperature until conversion was complete, then the solution was heated to 90° C. until gas evolution stopped. 3.4 mL of benzyl alcohol were added and stirring at 90° C. was continued for another 18 h. The mixture was allowed to cool down to room temperature and 500 mL of ethyl acetate were added. The organic layer was extracted two times with 1N HCl and once with brine, dried over magnesium sulfate and evaporated to dryness. The crude product was purified by silica gel chromatography to give 2.85 g of the desired product. Rt=2.52 min (Method E). Detected mass: 386.2 (M+1H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710077B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-8b7e43a254024eafab7deaeb59782eb3 |
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| Source note | uspto-grants-2014_04 |
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