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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethyl(2-heptafluoropropylbenzoxazol-5-yl)acetateHCID 22742119—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(2-heptafluoropropylbenzoxazol-5-yl)propionateHCID 22742104101.6%

Reaction Conditions

Temperature-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703347B2
Source datasetuspto-grants-2004_03
ORD IDord-b1bb050d246141e783166e53c8abf1ee
Source noteuspto-grants-2004_03