Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781235Generated: October 30, 2026

Water → HCID 19045060, compound

https://huagongshe.com/reaction/1781235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ChlorideHCID 5234—
ReactantDiketeneHCID 12661—
Reactant2-Bromo-4-methyl-6-nitroanilineHCID 2775306—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventButyl ChlorideHCID 8005—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19045060HCID 1904506046%

Reaction Steps

A solution of diketene (57.71 mL, 748.2 mmol) was added dropwise over 2 h to a stirred solution of title compound of Step A (34.57 g, 149.6 mmol) and 4-dimethylaminopyridine (914 mg, 7.48 mmol) in dry tetrahydrofuran (450 mL) at room temperature under a nitrogen atmosphere. The reaction was allowed to stir at room temperature overnight. First, water was added to the reaction, and then the reaction mixture was poured into water. The mixture was saturated with sodium chloride and was extracted with ethyl acetate three times. The combined organic layers were dried (MgSO4), filtered, and the solvent was removed under reduced pressure to give a brown oil. The brown oil was suspended in 1-chlorobutane. The resultant precipitate was filtered from this suspension to afford the title compound of Step B as a brown solid melting at 136°-138° C. (21.67 g, 46%). 1H NMR (CDCl3): δ2.35 (s,3H), 2.41 (s,3H), 3.63 (s,2H), 7.69 (s,2H), 9.6 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633218
Source datasetuspto-grants-1997_05
ORD IDord-8b376187240b4ed782555b182275be4f
Source noteuspto-grants-1997_05