Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Ethylhexanoic Acid | HCID 8697 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Product | HCID 20558300 | HCID 20558300 | 17.6% |
Reaction Steps
To 100 gm of 2-ethylhexanoic acid (0.693 moles) was added 247.5 g of thionyl chloride (2.080 moles) over 30 min. The solution was then heated at 70° for 2 hours. To the cooled solution was added 185.2 gm of N-chloro succinimide (1.387 moles), 165.0 g of thionyl chloride (1.387 moles) and 2.0 ml of concentrated HCl. The mixture was heated at 80° for 2 hours, after which time there was no more apparent Cl2 gas being given off. The mixture was cooled and filtered. The filtrate was distilled at atmospheric pressure to remove the SOCl2 and then distilled to give a major fraction at 95°-105° C. (20 mm) weighing 28.00 gm. Purity was determined by GLC analysis. Purity (area %) was 85.7%; yield was 17.6%. NMR showed no detectable extra chlorination.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04302569 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-97f1118481ed4151a8f2dd439bff47b4 |
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| Source note | uspto-grants-1981_11 |
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