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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869058Generated: October 26, 2026

Acetic Anhydride → HCID 18542894, compound

https://huagongshe.com/reaction/869058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1,3-Benzenediamine, 5-chloro-HCID 73335—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 18542894HCID 18542894—

Reaction Steps

DMAP (50 mg) and acetic anhydride (3.9 g, 37.9 mmol) were added sequentially and dropwise to a cold solution of 5-chloro-benzene-1,3-diamine (4.5 g, 31.6 mmol) in pyridine (22 mL) keeping the internal temperature below 0° C. The reaction mixture was allowed to warm to rt, stirred for 2 h, cooled to 0° C., quenched by addition of ice cooled water, and extracted with EtOAc. The organic phase was washed with brine, dried (Na2SO4), filtered, and concentrated. The crude material was purified by silica gel column chromatography (CH2Cl2/MeOH, 99:1) to afford the title compound. tR: 0.18 min (LC-MS 2); ESI-MS: 184.9 [M+H]+ (LC-MS 2); Rf=0.32 (hexane/EtOAc, 1:4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969341B2
Source datasetuspto-grants-2015_03
ORD IDord-c97cc895a31047a3bb4c7499ca828f09
Source noteuspto-grants-2015_03