HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864377Generated: October 25, 2026
Iodine → Ethyl 4-methoxy-3,5-dimethylbenzoate
https://huagongshe.com/reaction/864377
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-Bromo-2,6-dimethylanisole | HCID 278654 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-methoxy-3,5-dimethylbenzoate | HCID 53404664 | — |
Reaction Steps
A solution of 4-bromo-2,6-dimethylanisole (PREPARATION 1, 12.98 g) in tetrahydrofuran (40 ml) is added drop by drop to a mixture of magnesium turnings (1.87 g) in tetrahydrofuran (5 ml). The Grignard reaction is initiated with iodine crystals. After the addition is complete, the mixture is refluxed for 2 hours. The Grignard reagent is cooled to about 10° and then a solution of ethyl chloroformate (7.5 ml) in tetrahydrofuran (40 ml) is added in a 2 minute period. The mixture is stirred for 45 minutes at ice-water temperature and then at 20°-25° for 2 hours. The reaction is quenched with a saturated solution of ammonium chloride and diluted with ether. The phases are separated, the organic phase is washed with water and then with saline, dried over sodium sulfate, and concentrated under reduced pressure to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05563142 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-217bdb3ac8884d87a4cfc49d7a066f65 |
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| Source note | uspto-grants-1996_10 |
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