HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658960Generated: October 30, 2026
Imidazole → (E)-ethyl 7-(tert-butyldimethylsiloxy)-2-methyl-2-heptenate
https://huagongshe.com/reaction/658960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (E)-ethyl 7-hydroxy-2-methyl-2-heptenate | HCID 10559469 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-ethyl 7-(tert-butyldimethylsiloxy)-2-methyl-2-heptenate | HCID 11055704 | 98.8% |
Reaction Steps
To a methylene chloride solution (300 ml) of Ester 3 (13.91 g; 0.0748 mol), 43 ml of DMF (dimethylformamide) and imidazole (7.6 g; 0.112 mol) are added and the whole is stirred until imidazole is fully dissolved. Tert-butyldimethylsilyl chloride (13.5 g; 0.0897 mol) is then added thereto and the whole is stirred for 20 min. After stirring, the resultant solution is quenched using a buffer solution (100 ml) and the organic compound is extracted three times with ethyl acetate, followed by the wash of the organic layer in a saturated saline solution and drying over anhydrous magnesium sulfate. After anhydrous magnesium sulfate is filtered and the solvent is distilled off under reduced pressure, the residue is separated and purified by column chromatography (developing solution, ethyl acetate:hexane=1:1) to produce Ester 4 (22.16 g; 0.0739 mol) of 99% in yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE043038E1 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-562ee5a0ecad40a38ec6091b3810ad52 |
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| Source note | uspto-grants-2011_12 |
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