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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033822Generated: October 31, 2026

Acetone → {[(2-Methyl-1-nitropropan-2-yl)sulfanyl]methyl}benzene

https://huagongshe.com/reaction/1033822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantNitromethaneHCID 6375—
ReactantBenzyl mercaptanHCID 7509—
ReactantPiperidineHCID 8082—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product{[(2-Methyl-1-nitropropan-2-yl)sulfanyl]methyl}benzeneHCID 14613816—

Reaction Steps

Acetone (25 g), benzyl mercaptan (53 g), nitromethane (26.2 g), and piperidine (8 cm3) were dissolved in benzene (150 cm3) and the mixture heated under reflux with azeotropic removal of water. After 48 h the reaction mixture was allowed to cool and washed first with dilute hydrochloric acid, then with water. The remaining solution was dried (MgSO4) and the solvent then removed under reduced pressure to give the nitro system (76.5 g, 85%). This material was sufficiently pure to be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312904
Source datasetuspto-grants-1994_05
ORD IDord-f1507ad9f5b4440ba0987a3e0f60a33b
Source noteuspto-grants-1994_05