Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601277Generated: October 29, 2026

Benzyl mercaptan → 4-(Benzyloxy)-2-(benzylthio)-1-nitrobenzene

https://huagongshe.com/reaction/601277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantSodium CarbonateHCID 10340—
Reactant4-Benzyloxy-2-fluoro-1-nitrobenzeneHCID 22180704—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(Benzyloxy)-2-(benzylthio)-1-nitrobenzeneHCID 67063443100.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

A slurry of the product of Example 304A (15 g, 0.061 mol) in ethanol (100 mL), was treated with sodium carbonate (6.41 g, 0.061 mol) and benzyl mercaptan (7.5 mL, 0.058 mol) in water (50 mL). The reaction mixture was refluxed for 5 hours, cooled to 25° C. and poured into of distilled water (800 mL). The resulting slurry was stirred forl hour at 25° C. and filtered. The resulting yellow solid was washed with water and dried in a vacuum oven at 50° C. to give the title compound (20.53 g). 1H NMR (300 MHz, DMSO-d6) δ ppm 4.35 (s, 2 H) 5.27 (s, 2 H) 7.02 (dd, J=9.19, 2.57 Hz, 1 H) 7.16 (d, J=2.57 Hz, 1 H) 7.40 (m, 10 H) 8.24 (d, J=9.19 Hz, 1 H). ESI m/z (M+H)+: 352

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902203B2
Source datasetuspto-grants-2011_03
ORD IDord-4fce084d907f47cc98076dbc63873733
Source noteuspto-grants-2011_03