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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1,4-Dioxaspiro[4.5]decane-8-carboxylic acid, 8-(4-fluorophenyl)-HCID 12230246—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product[8-(4-Fluoro-phenyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-carbamic acid benzyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710077B2
Source datasetuspto-grants-2014_04
ORD IDord-8b7e43a254024eafab7deaeb59782eb3
Source noteuspto-grants-2014_04