HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48164Generated: October 29, 2026
Methyl iodide → Methyl 2-(2-heptafluoropropylbenzoxazol-5-yl)propionate
https://huagongshe.com/reaction/48164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Methyl(2-heptafluoropropylbenzoxazol-5-yl)acetate | HCID 22742119 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(2-heptafluoropropylbenzoxazol-5-yl)propionate | HCID 22742104 | 101.6% |
Reaction Steps
A solution of lithium diisopropylamide (2.0M solution in tetrahydrofuran/ethyl benzene/heptane, 15.32 ml, 0.0306 mol) was added dropwise to a solution of methyl(2-heptafluoropropylbenzoxazol-5-yl)acetate (11.0 g, 0.0306 mol) in tetrahydrofuran (175 ml) at −70° C. under a nitrogen atmosphere and the mixture was stirred at −70° C. for 1 hour. A solution of methyl iodide (39.1 g, 0.275 mol) in tetrahydrofuran (25 ml) was added dropwise and the mixture was stirred at −70° C. for a further 1 hour. The cooling bath was removed and the mixture was allowed to warm to room temperature over a period of 3 hours. The reaction was quenched with water, acidified with dilute aqueous hydrochloric acid and extracted with ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate was evaporated in vacuo to give methyl 2-(2-heptafluoropropylbenzoxazol-5-yl)propionate (11.6 g) as a reddish oil, which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06703347B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-b1bb050d246141e783166e53c8abf1ee |
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| Source note | uspto-grants-2004_03 |
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