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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325657Generated: October 30, 2026

Tert-Butylamine → HCID 13136802, compound

https://huagongshe.com/reaction/325657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantHCID 13136801HCID 13136801—
SolventEthanolHCID 702—
ProductHCID 13136802HCID 13136802—

Reaction Steps

7.5 gm (0.024 mol) of 1-(2-cyano-4-cyclobutylcarbonylamino-phenoxy)-3-chloro-propan-2-ol were dissolved in 80 ml of ethanol, and the solution was mixed with 8.7 gm (0.12 mol) of tert. butylamine, and the mixture was refluxed for four hours. The solvent was distilled off in vacuo, the residue was extracted by shaking with dilute hydrochloric acid with the addition of ether, and the organic phase was separated. The aqueous phase was washed with ether and made alkaline with NH4OH. The base which precipitated was extracted with ethyl acetate, and the organic phase was dried over MgSO4. The ethyl acetate was distilled off, and the crystalline residue was recrystallized twice from acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04442120
Source datasetuspto-grants-1984_04
ORD IDord-84f3971879654b8f81e2b6a2f069b091
Source noteuspto-grants-1984_04