Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58284813 | HCID 58284813 | — |
Reaction Steps
Charged aluminum chloride (183 mmoles), pentanoyl chloride (147 mmoles) and bromothiophene (122 mmoles) to the RB flask fitted with thermo well, stirred the reaction for 2 hours at 25-30° C. After completion of reaction, cooled the RM to 0-5° C. and added Water (100 ml). Extracted the reaction mass with ethyl acetate (2×200 ml), separated the organic layer and dried with sodium sulphate, distilled off the solvent under reduced pressure to the residue. Residue was high vacuum distilled to get the pure compound (XXI).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703811B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-ec9bb26064454851a322a419c63ba29a |
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| Source note | uspto-grants-2014_04 |
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