HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973267Generated: October 31, 2026
1-Iodo-3-methylbutane → HCID 21402622, compound
https://huagongshe.com/reaction/973267
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Iodo-3-methylbutane | HCID 10924 | — |
| Reactant | ethyl 5-hydroxy-4-oxo-4H-chromene-2-carboxylate | HCID 2801504 | — |
| Reactant | Thallium | HCID 5359464 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21402622 | HCID 21402622 | — |
Reaction Steps
A stirred mixture of 21.67 parts of ethyl 5-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylate, thallium salt and 99 parts of 1-iodo-3-methylbutane was refluxed for one hour. After cooling, chloroform was added to the reaction mixture and the insoluble thallium salts were removed by filtration. The chloroform filtrate was washed with cold N sodium hydroxide solution, then washed with water and the volatile components were removed by evaporation. Sodiumbicarbonte soluton was added to the oily residue obtained and the mixture was stirred at 100° C for 2 hours. After cooling, the solution ws extracted with chloroform and the aqueous layer was separated. This aqueous extract was acidified with 2H hydrochloric acid and the solid which precipitated was collected by filtration, washed with water and dried to give 6.16 parts of 5-(3-methyl-n-butoxy)-4-oxo-4H-1-benzopyran-2-carboxylic acid, m.p. 181°-183° C (after crystallistion from ethyl acetate/light petroleum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04055654 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-a692ffbb1cbd455a95eb28441e465954 |
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| Source note | uspto-grants-1977_10 |
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