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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503188Generated: October 30, 2026

Tetrahydrofuran → HCID 66868325, compound

https://huagongshe.com/reaction/1503188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactantp-TrifluoromethylpropiophenoneHCID 136554—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantTrimethylphosphonoacetateHCID 53413272—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 66868325HCID 6686832585%

Reaction Steps

To a chilled (0° C.) solution of lithium bis(trimethylsilyl)amide (1.0 M, 50 mL) was dropwise added a solution of trimethylphosphonoacetate, keeping the temperature below 10° C. The solution was then allowed to warm to room temperature and stirred for an additional five minutes, after which a solution of 4′-(trifluoromethyl)propiophenone in THF (25 mL) was added in one portion. The solution was slowly heated to 50° C. for eight hours. The solution was cooled to room temperature, then diluted with a 10% NH4Cl solution (100 mL), and extracted with ethyl acetate (2×100 mL). The organic layers were combined and dried over MgSO4, filtered, and the filtrate concentrated to a white solid which was recrystallized from hexane/ethyl acetate to give 5.42 grams of 3-(4-trifluoromethylphenyl)pent-2-enoic acid methyl ester intermediate (85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212155B2
Source datasetuspto-grants-2015_12
ORD IDord-aa09d9f66c7e4cf6be3e60dd6bacbff9
Source noteuspto-grants-2015_12