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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172884Generated: November 1, 2026

Water → Di-tert-butyl [4-(1,3-dioxolan-2-yl)-3-fluorophenyl](methyl)malonate

https://huagongshe.com/reaction/1172884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantDi-tert-butyl [4-(1,3-dioxolan-2-yl)-3-fluorophenyl]malonateHCID 57443964—
SolventDimethylformamideHCID 6228—
ProductDi-tert-butyl [4-(1,3-dioxolan-2-yl)-3-fluorophenyl](methyl)malonateHCID 57443965—

Reaction Conditions

Temperature70 °C

Reaction Steps

Di-tert-butyl[4-(1,3-dioxolan-2-yl)-3-fluorophenyl]malonate (2.45 g, 6.41 mmol), iodomethane (0.80 mL, 12.85 mmol) and potassium carbonate (1.78 g, 12.9 mmol) were suspended in DMF (10 mL) and heated at 70° C. for 3 hours in a sealed tube. A further portion of iodomethane was added (0.60 mL, 9.64 mmol) and heating continued at 75° C. for 3 hours. Room temperature was attained, H2O (150 mL) was added and the products extracted into Et2O (2×100 mL). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification of the residue by MPLC gave the clean product (orange oil). 1H NMR (CDCl3) δ 7.47 (t, J=8.1 Hz, 1H), 7.19 (dd, J=8.1, 1.8 Hz, 1H), 7.17 (dd, J=12.0, 1.8 Hz, 1H), 6.07 (s, 1H), 4.13 (m, 2H), 4.03 (m, 2H), 1.74 (s, 3H), 1.45 (s, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834034B2
Source datasetuspto-grants-2010_11
ORD IDord-78fa2697d70c41df90c7c7ee8672d93d
Source noteuspto-grants-2010_11