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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527443Generated: November 5, 2026

Sodium Azide → (1R,3S,5R)-3-Azidomethyl-2-aza-bicyclo[3.1.0]hexane-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1527443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant(1R,3S,5R)-3-(Toluene-4-sulfonyloxymethyl)-2-aza-bicyclo[3.1.0]hexane-2-carboxylic acid tert-butyl esterHCID 86673858—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product(1R,3S,5R)-3-Azidomethyl-2-aza-bicyclo[3.1.0]hexane-2-carboxylic acid tert-butyl esterHCID 86673859—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of (1R,3S,5R)-3-(toluene-4-sulfonyloxymethyl)-2-aza-bicyclo[3.1.0]hexane-2-carboxylic acid tert-butyl ester (0.400 g, 1.08 mmol) and NaN3 (0.420 g, 6.47 mmol) in dry DMSO (8 mL) was stirred at 65° C. overnight. After cooling, the mixture was diluted with Et2O and washed with water (×3) and brine (×2). The organics were dried (phase separator) and concentrated in vaccuo to give the title compound as a colorless oil. MS (LC-MS): 239.0 [M+H]+; tR (HPLC conditions k): 3.78 min. The material thus obtained was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-e51d3cc078b94720a911f89c465556c5
Source noteuspto-grants-2015_07