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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372901Generated: October 29, 2026

Ammonia → HCID 18759733, compound

https://huagongshe.com/reaction/2372901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ProductHCID 18759733HCID 1875973342%

Reaction Steps

To a stirred solution of 1.21 g (7.02 mmol) of Part A(4) compound in 50 mL of toluene was added 3 mL (134 mmol) of oxalyl chloride. The reaction mixture was stirred for 1 hour at room temperature under argon and then concentrated in vacuo. The residue was diluted with 20 mL of toluene and concentrated again. This was repeated to remove traces of oxalyl chloride. The residue of the crude acid chloride was stirred in 5 mL of methanol and then 1.17 mL (8.43 mmol) of triethylamine and 2 mL (9M, 18 mmol) of methanolic ammonia were added at room temperature under argon. After stirring for 16 hours, the reaction mixture was partitioned between 3 mL water and 20 mL ethyl acetate. The organic layer was separated and the aqueous layer was extracted twice with ethyl acetate (20 mL). The combined organic layers were washed with brine then dried (magnesium sulfate) and concentrated in vacuo to obtain a semi-solid. The semi-solid was crystallized by trituration with hexane to obtain 0.5 g (42%) of title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100889
Source datasetuspto-grants-1992_03
ORD IDord-b22ea5dcf6734c808914e93790705b21
Source noteuspto-grants-1992_03