HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10120Generated: October 29, 2026
Dimethylformamide → 7-methyl-9-oxo-thioxanthene-3-carbonyl Chloride
https://huagongshe.com/reaction/10120
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 7-Methyl-9-oxothioxanthene-3-carboxylic acid | HCID 10825905 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-methyl-9-oxo-thioxanthene-3-carbonyl Chloride | HCID 10850940 | 85% |
Reaction Steps
The 7-methyl-9-oxothioxanthene-3-carboxylic acid (MTA), 50.0 g (0.185 mol), was dissolved in 350 ml of toluene and 415 ml (5.69 mol) of thionyl chloride using an overhead stirrer in a 2 liter 3-neck round bottom flask. N,N-Dimethylformamide (DMF), 2 ml, was added and the reaction was brought to reflux for 2 hours. After this time, the mixture was stirred at room temperature for 16 hours. The solvent was removed under vacuum and the product was azeotroped with 3×350 ml of toluene to remove the excess thionyl chloride. The product was recrystallized from 800 ml of chloroform and the resulting solid was placed in a vacuum oven for 16 hours at 45° C. to complete removal of solvent. The isolated product weighed 45.31 g (85% yield) and nuclear magnetic resonance spectroscopy (NMR) confirmed the desired structure. This product was used for the preparation of a photoreactive monomer as described in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094418B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-4f7b41588ad642d29308ad28a09d5a18 |
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| Source note | uspto-grants-2006_08 |
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