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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37450Generated: October 30, 2026

Acetic Anhydride → HCID 178454361, compound

https://huagongshe.com/reaction/37450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantMaleic AnhydrideHCID 7923—
ReactantTriethylamineHCID 8471—
Reactant2-BOC-hydrazino-5-amino pyridineHCID 10376339—
CatalystCobalt diacetateHCID 6277—
SolventAcetoneHCID 180—
ProductHCID 178454361HCID 17845436128.3%

Reaction Steps

To a stirred solution of 2-BOC-hydrazino-5-amino pyridine (1 equivalent) in acetone (50 ml/gm) was added maleic anhydride (1.1 equivalents). The reaction mixture was stirred at 25° for 2 hours. To the reaction mixture was added acetic anhydride (1.2 equivalents), cobalt acetate (0.007 equivalents) and triethylamine (0.3 equivalents). The reaction mixture was stirred at 60° for 2 hours. The color of the reaction began as bright yellow and ended as dark yellow. The reaction mixture was concentrated under reduced pressure to give a yellow brown oil. Flash vacuum chromatography (hexanes/ethyl acetate (8/2)) was used to isolate the product. The product was recrystallized in ether/hexane; yield 28.3%; m.p. 182°-184°. IR (KBr): 3400, 3300, 3100, 2990, 1700, 1610, 1500, 1410, 1360, 1320, 1270, 1210, 1150, 1050, 830, 750, 690 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420285
Source datasetuspto-grants-1995_05
ORD IDord-a9e1d90b102749fab1342dfcf79bf561
Source noteuspto-grants-1995_05