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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651580Generated: October 30, 2026

Phenylhydrazine → HCID 15886886, compound

https://huagongshe.com/reaction/651580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHCID 21709029HCID 21709029—
ProductHCID 15886886HCID 15886886—

Reaction Conditions

Temperature170 °C

Reaction Steps

N,N-Dihexyl-(4-oxo-thiochroman-2-yl)-carboxamide (1.00 g) and phenylhydrazine (0.26 ml) were stirred at 100° C. for 30 minutes, and the reaction mixture was dried under reduced pressure at 50° C. for 30 minutes. The residue, after addition of 1.44 g of anhydrous zinc chloride, was stirred at 170° C. for 5 minutes, and cooled to room temperature. To the reaction mixture was added ice water, followed by extracting with ethyl acetate. The extract was washed with 1N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the filtrate was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-hexane to give 0.79 g of N,N-dihexyl-6,11-dihydro-5-thia-11-aza-benzo[a]fluoren-6-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281355B1
Source datasetuspto-grants-2001_08
ORD IDord-b9cbada24e5e43cb84d2ff9b8eb10e10
Source noteuspto-grants-2001_08