Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336837Generated: October 26, 2026

tert-Butanol → 937040-09-0

https://huagongshe.com/reaction/336837

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantDiphenylphosphoryl azideHCID 123414—
Reactant5-Nitro-1H-pyrazole-3-carboxylic acidHCID 86222684—
Product937040-09-0HCID 135971896—

Reaction Steps

To 10 g (63.66 mmol) of 5-nitro-1H-pyrazole-3-carboxylic acid are respectively added 39 ml of tert-butanol, 27.44 ml (127.3 mmol) of diphenylphosphorazidate and 17.7 ml (127.32 mmol) of triethylamine. The solution is refluxed for 8 h, then an aqueous solution saturated with potassium carbonate is added until reaching pH 8, and the product is extracted several times with ethyl acetate. The organic phases are combined, dried over magnesium sulfate, and concentrated. The residue obtained is triturated in methanol to give 4.38 g of tert-butyl 5-nitro-1H-pyrazol-3-ylcarbamate in the form of a yellow solid. The filtrate is concentrated and purified by chromatography on silica (cyclohexane/ethyl acetate eluent: 7:3) to yield an additional 1.49 g of tert-butyl 5-nitro-1H-pyrazol-3-ylcarbamate in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889711B2
Source datasetuspto-grants-2014_11
ORD IDord-52f8fe2e15e2415694cb6554a8830328
Source noteuspto-grants-2014_11