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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39419Generated: October 26, 2026

Water → trans-(4-Azido-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/39419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium AzideHCID 33557—
ReactantLithium perchlorateHCID 23665649—
ReactantTert-butyl 3-oxa-7-azabicyclo[4.1.0]heptane-7-carboxylateHCID 58381262—
SolventAcetonitrileHCID 6342—
Producttrans-(4-Azido-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl esterHCID 8665633852.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Oxa-7-aza-bicyclo[4.1.0]heptane-7-carboxylic acid tert-butyl ester (intermediate E) (5.2 g, 26 mmol) was dissolved in 100 mL acetonitrile. Lithium perchlorate (23 g, 207 mmol) and sodium azide (6.8 g, 104 mmol) were added and the reaction mixture was stirred at 80° C. overnight. 200 mL Water was added. The mixture was extracted three times with diethylether. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (heptane/ethyl acetate 1:0→1:1) yielded the title compound as a colorless oil (3.3 g, 52%), MS: m/e=186 [(M-butene)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524909B2
Source datasetuspto-grants-2013_09
ORD IDord-5c9dd2f5be3748d3b48fc749a9973630
Source noteuspto-grants-2013_09