HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058653Generated: October 31, 2026
Sodium Hydroxide → 2-[(2-Chlorophenyl)sulfanyl]-5-nitrobenzaldehyde
https://huagongshe.com/reaction/1058653
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | o-Chlorothiophenol | HCID 80599 | — |
| Reactant | 2-Fluoro-5-nitrobenzaldehyde | HCID 2734770 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[(2-Chlorophenyl)sulfanyl]-5-nitrobenzaldehyde | HCID 18668999 | 85.1% |
Reaction Steps
A 2.5 mol/L sodium hydroxide aqueous solution (1.7 mL, 4.4 mmol) and tetrabutylammonium bromide (0.017 g, 0.051 mmol) were added to 2-chlorobenzenethiol (0.17 g, 1.0 mmol), followed by stirring at 25° C. for 10 minutes. To the reaction liquid was added a toluene (1.7 mL) solution of 2-fluoro-5-nitrobenzaldehyde (0.18 g, 1.0 mmol), followed by stirring at 110° C. for 2 hours. After the conventional post-reaction treatment, the residue was purified by silica gel chromatography (eluted by chloroform) to give 2-[(2-chlorophenyl)thio]-5-nitrobenzaldehyde (0.25 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518268B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-b1d3b367fdf04450b920786fa93d2ed6 |
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| Source note | uspto-grants-2003_02 |
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