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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386045Generated: November 1, 2026

3-Nitrobenzaldehyde → HCID 9929475, compound

https://huagongshe.com/reaction/1386045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
Reactant3-Aminocyclohex-2-en-1-oneHCID 78892—
ReactantDihydro-2H-thiopyran-3(4H)-one-1,1-dioxideHCID 11815935—
SolventEthanolHCID 702—
ProductHCID 9929475HCID 9929475—

Reaction Steps

A solution of 3-nitrobenzaldehyde (151 mg, 1.00 mmol), tetrahydrothiopyran-3-one-1,1-dioxide (148 mg, 1.00 mmol), prepared according to the method described in J. Heterocycl. Chem. (1990), 27, 1453, and 3-amino-2-cyclohexen-1-one (111 mg, 1.00 mmol) in ethanol (7 mL) was heated at reflux for 24 hours and cooled. The solid that precipitated was washed with ethanol, dried, and triturated with hot methanol to provide the title compound. MS (APCI) m/e 375 (M+H)+; 1H NMR (DMSO-d6) 1.75 (m, 1H), 1.90 (m, 1H), 2.22 (m, 4H), 2.55 (m, 4H), 3.22 (m, 2H), 5.15 (s, 1H), 7.55 (t, 1H), 765 (d, 1H), 8.00 (m, 1H), 9.48 (br s, 1H); Anal. Calcd for C, 57.74; H, 4.85; N, 7.48. Found: C, 57.41; H, 4.75; N, 7.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265417B1
Source datasetuspto-grants-2001_07
ORD IDord-ac138a6a6c6d405eafcf0a1c3e22729c
Source noteuspto-grants-2001_07