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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597167Generated: October 30, 2026

Acetic Acid → HCID 20304652, compound

https://huagongshe.com/reaction/597167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperonylamineHCID 2723901—
ReactantHCID 12233800HCID 12233800—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
ProductHCID 20304652HCID 20304652—

Reaction Steps

Glacial acetic acid (700 ml) is added dropwise to a vigorously stirred mixture of 62 g of 2,3,4,5-tetrahydro-5-nitroso-1,5-benzothiazepine, 49 g of 4-piperidone hydrochloride monohydrate, 400 ml of anhydrous ethanol, and 140 g of zinc dust, cooled in an ice-bath. After the addition is complete, the mixture is stirred at room temperature for 1 hr. and filtered. The residue is washed with a small quantity of ethanol and the combined filtrates heated at 65°-70° C for 1 hour and then stripped of ethanol and acetic acid under reduced pressure. The residual viscous liquid is dissolved in minimum quantity of water and added with stirring, to excess of well-cooled 25% aqueous sodium hydroxide. The mixture is thoroughly extracted with chloroform and the combined chloroform extracts washed well with water, dried over anhydrous magnesium sulfate and stripped of the solvent under reduced pressure. The residue on trituration with ether and cooling yields 2,3,4,5-tetrahydro-5-[(4-piperidylidene)amino]-1,5-benzothiazepine as cream colored crystals, m.p. 113°-115°. A sample of this hydrazone melts at 115°-117° C. after recrystallization from a mixture of benzene and hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04013652
Source datasetuspto-grants-1977_03
ORD IDord-74438c1209c54bcaa610f0866030a500
Source noteuspto-grants-1977_03