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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891735Generated: October 28, 2026

Sodium Azide → HCID 22242898, compound

https://huagongshe.com/reaction/891735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant3-Methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)azetidineHCID 22242857—
SolventDimethylformamideHCID 6228—
ProductHCID 22242898HCID 2224289855.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)azetidine (4.63 g, 14.0 mmol) (obtained as described in Reference Example 54(2)) in dimethylformamide (140 ml) was added sodium azide (1.37 g, 21.0 mmol), and the mixture was stirred in an oil bath (100° C.) for 4 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (2:1→1:1) as the eluant to afford 3-azido-1-(p-nitrobenzyloxycarbonyl)azetidine (2.15 g, yield 55%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-e7bc774f853649a788db06976045a7a6
Source noteuspto-grants-2006_02