HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918103Generated: October 31, 2026
Thionyl Chloride → HCID 54543855, compound
https://huagongshe.com/reaction/918103
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21522824 | HCID 21522824 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54543855 | HCID 54543855 | — |
Reaction Steps
11.7 g. of (2-phenyl-5-chloro-1,3-benzodioxol-2-yl)-acetic acid mixed with 50 cc. of anhydrous benzene are refluxed with 10 cc. of SOCl2 for 3 hours. The solvent and the excess of SOCl2 are removed under vacuum. The residual oil mixed with 150 cc. of anhydrous ether is added in drops to an ether solution of diazomethane, which is ice cooled to maintain the temperature under 2°-3°C. After 24 h, the ether is removed under vacuum and the residue is mixed with 100 cc. of ethanol. The mixture is heated at 50°C., and 2 g. of Ag2O are added. After 2 hours, the product is treated with animal charcoal, filtered and dried. It is then fractionated and the desired product boils at 200°-207°C./0.4 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03969368 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-d92f4c735836404baf0ea9fa7e23b3ad |
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| Source note | uspto-grants-1976_07 |
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