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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127567Generated: October 31, 2026

Hydrochloric Acid → HCID 136335641, compound

https://huagongshe.com/reaction/127567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 12747240HCID 12747240—
SolventPyridineHCID 1049—
ProductHCID 136335641HCID 136335641—

Reaction Steps

A mixture of 50.00 g of the product mixture from the stannous chloride reduction of 10-nitro-5H-dibenzo[a,d]cyclohepten-5-one and 62.61 g (0.901 mol) of hydroxylamine hydrochloride in 500 ml of pyridine was refluxed for 6 hr, poured into 3000 ml of ice water and 100 ml of conc. HCl, and extracted with CH2Cl2. The extracts were washed with brine, dried, treated with activated charcoal, filtered, and concentrated in vacuo to give a solid suspended in pyridine. The solid was removed by filtration and the pyridine treated as above to give a white solid. The solids were combined giving 44.09 g of 5,10-dioximino-10,11-dihydro-5H-dibenzo[a,d]cycloheptene as a white solid which had incorporated pyridine. The pyridine could not be removed by heating, high vacuum, or recrystallization: mp 220°-221°; NMR (DMSO-d6 /TMS) δ 11.62 (s, 1H, =NOH), 11.57 (s, 1H, =NOH), 7.50-7.00 (m, 8H, arom), and 3.97 (br s, 2H, benzylic); IR (CHCl3) 2.79, 3.34, 6.33, 6.99, 8.20, 8.34, 9.39, 9.74, 10.09, 10.79, 12.65 and 14.34μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256742
Source datasetuspto-grants-1981_03
ORD IDord-cf76da4abd5f4759a2252aaa20b52bdc
Source noteuspto-grants-1981_03