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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856556Generated: October 31, 2026

Tetrahydrofuran → HCID 23345204, compound

https://huagongshe.com/reaction/1856556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Nitrophenyl isothiocyanateHCID 137690—
ReactantHCID 23345092HCID 23345092—
SolventEthanolHCID 702—
ProductHCID 23345204HCID 2334520484%

Reaction Steps

A mixture of 21.6 parts of 1-isothiocyanato-2-nitrobenzene and 45 parts of tetrahydrofuran is stirred till all solid enters solution. Then there are added 29.5 parts of N-(1-methylethyl)-1-(2-phenylethyl)-4-piperidinamine and 160 parts of ethanol and the whole is stirred overnight at room temperature. The reaction mixture is evaporated and the residue is crystallized from 2-propanol. The product is filtered off and dried, yielding 43 parts (84%) of N-(1-methylethyl)-N'-(2-nitrophenyl)-N-[1-(2-phenylethyl)-4-piperidinyl]thiourea; mp. 100.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04219559
Source datasetuspto-grants-1980_08
ORD IDord-ebf9f2a14bc8428eb401548378b0da6e
Source noteuspto-grants-1980_08