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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792343Generated: November 4, 2026

Sodium Azide → 4,4,5,5,5-Pentafluoropentylcarbamic acid t-butylester

https://huagongshe.com/reaction/1792343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant4,4,5,5,5-Pentafluoropentyl 4-methylbenzenesulfonateHCID 22033027—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4,4,5,5,5-Pentafluoropentylcarbamic acid t-butylesterHCID 2353806650%

Reaction Conditions

Temperature60 °C

Reaction Steps

1,1,1,2,2-Pentafluoro-5-p-toluenesulfonyloxypentane (4.00 mg, 12.0 mmol) was dissolved in methanol (40 ml), NaN3 (936 mg, 14.4 mmol) dissolved in water (10 ml) was added thereto, and the mixture was stirred overnight at 60° C. After the reaction was completed, the reaction mixture was extracted with chloroform and washed with saturated saline solution. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in methanol (40 ml), (Boc)2O (2.62 g, 12.0 mmol) and Pd—C (800 mg) were added thereto, and then the mixture was stirred overnight under hydrogen. After the reaction was completed, the mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (n-hexane:ethyl acetate=4:1) to give 4,4,5,5,5-pentafluoropentylcarbamic acid t-butylester (1.12 g, yield 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074819B2
Source datasetuspto-grants-2006_07
ORD IDord-1484ee4f8f4c4d37bc42d1884b092656
Source noteuspto-grants-2006_07