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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256160Generated: October 31, 2026

alpha-Methylene butyrolactone → HCID 86655229, compound

https://huagongshe.com/reaction/1256160

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Methylene butyrolactoneHCID 68352—
ReactantPotassium AcetateHCID 517044—
Reactant2,2,2-Trifluoro-N-(3-iodophenyl)acetamideHCID 18877657—
Catalystpalladium(II) acetateHCID 167845—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86655229HCID 8665522980.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

The reaction mixture of 2,2,2-trifluoro-N-(3-iodophenyl)acetamide (160 mg, 0.52 mmol), 3-methylenedihydrofuran-2(3H)-one (62 mg, 0.63 mmol), Pd(OAc)2 (33 mg, 0.015 mmol) and KOAc (200 mg, 2.04 mmol) in NMP (2 mL) was degassed and heated to 110° C. for 12 hrs. The mixture was extracted with EtOAc and washed with H2O, brine, dried over MgSO4, filtered, concentrated in reduced pressure to dryness, and recrystallized in MeOH to give desired intermediate (Z)-2,2,2-trifluoro-N-(3-((2-oxodihydrofuran-3(2H)-ylidene)methyl)phenyl)acetamide (120 mg). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 11.4 (s, 1H), 7.96 (s, 1H), 7.74 (dt, J=7.6, 1.6 Hz, 1H), 7.51 (7, J=7.6 Hz, 1H), 7.28 (d, J=8.4 Hz, 1H), 7.47 (dt, J=7.6, 1.6 Hz, 1H), 7.38 (t, J=2.8 Hz, 1H), 4.43 (t, J=7.2 Hz, 2H), 3.24 (dt, J=2.8, 7.2 Hz, 2H). MS (ESI) m/z=284 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-6b03a9673b464590898dcc2f52b1220d
Source noteuspto-grants-2013_06