HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003770Generated: October 27, 2026
Sulfuric Acid → 1,3-Diisobutyryloxy-2-(2,4-difluorophenyl)-2-propanol
https://huagongshe.com/reaction/1003770
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-Bromo-2,4-difluorobenzene | HCID 67674 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1,3-Diisobutyryloxyacetone | HCID 15521806 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Diisobutyryloxy-2-(2,4-difluorophenyl)-2-propanol | HCID 11290869 | 84.6% |
Reaction Steps
Under an atmosphere of argon, 5 ml of THF was slowly added to 925 mg of magnesium turnings, and then thereto was added dropwise 7 g of 2,4-difluorobromobenzene dissolved in 30 ml of THF with keeping the temperature at 20° C. After the reaction mixture was stirred for 1 hour with keeping the temperature at 20° C., 7.9 g of 1,3-diisobutyryloxyacetone dissolved in 10 ml of THF was added dropwise thereto with keeping the temperature at 0° C. After the dropping, the reaction mixture was stirred for 4 hours and then the reaction was stopped by adding 35 ml of 1N sulfuric acid. The obtained liquid was extracted twice with 35 ml of ethyl acetate. The organic layer was washed with saturated aqueous solution with sodium bicarbonate and with saturated aqueous solution with sodium chloride, in turn. The solvent was removed under reduced pressure. Thus obtained concentrate was distilled under reduced pressure to give 10 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046354 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-3278b5e9410e4af8881d8fc341c92994 |
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| Source note | uspto-grants-2000_04 |
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