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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983667Generated: October 30, 2026

Methyl formate → HCID 22561313, compound

https://huagongshe.com/reaction/983667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-(4'-Fluorophenyl)-1,3-DihydroIsobenzofuran-5-CarbonitrileHCID 9856159—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22561313HCID 2256131350%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile (2.4 g, 10 mmol) in THF (15 mL) was added to a solution of LDA (11 mmol) in THF (25 mL) at −78° C. under an atmosphere of nitrogen. The mixture was allowed to warm to −40° C. during 45 min. Freshly distilled methyl formate (0.75 mL, 12 mmol) was added at this temperature, and stirring was continued for 1 h while warming to 0° C. Then the mixture was poured into ice/saturated ammonium chloride solution, and extracted with Et2O (3×100 mL). The organic extracts were washed with brine, dried and evaporated. Silica gel chromatography (heptane, EtOAc 4:1) of the residue gave the product (1.3 g, 50%). 1H NMR (CDCl3) δ 5.35 (2H, s); 7.10 (2H, t, J=9.0 Hz); 7.50 (1H, dd, J=5.2 and 9.0 Hz); 7.57 (1H, s); 7.60 (1H, d, J=8.0 Hz); 7.70 (1H, d, J=8.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864379B2
Source datasetuspto-grants-2005_03
ORD IDord-0e5be1e8800245c2ae2b545c90adbeb2
Source noteuspto-grants-2005_03