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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005980Generated: October 31, 2026

tert-Butanol → HCID 69926284, compound

https://huagongshe.com/reaction/1005980

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 22674259HCID 22674259—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69926284HCID 69926284357.2%

Reaction Steps

To a solution of 1.90 g (6.88 mmol) 2-methylsulfanyl-4-o-tolyloxy-pyrimidine-5-carboxylic acid, 0.95 ml triethylamine (6.88 mmol) and 1.29 ml (1.37 mmol) t-butanol in 25 ml THF, 1.47 ml (6.88 mmol) diphenylphosphorylazide were added and the resulting solution heated at reflux for 12 hrs. After evaporation of the solvent, the residue was distributed between CH2Cl2 and H2O. The aquoeus phase was extracted twice with 80 ml CH2Cl2. The combined organic layers were dried (Na2SO4), filtered and evaporated. The residue was purified by chromatography (SiO2, CH2Cl2, ethyl acetate 40:1) to give 1.70 g (71%) (2-methylsulfanyl-4-o-tolyloxy-pyrimidin-5-yl)-carbamic acid tert.-butyl ester as a colorless solid, MS (ISP): 348.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787539B2
Source datasetuspto-grants-2004_09
ORD IDord-5c566e7128214bab9b9191cbd2f9bcb2
Source noteuspto-grants-2004_09