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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214916Generated: October 30, 2026

Dimethylformamide → HCID 14708119, compound

https://huagongshe.com/reaction/2214916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 86596744HCID 86596744—
ReactantHCID 178418306HCID 178418306—
ProductHCID 14708119HCID 1470811956%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a chilled (−78° C.), stirred solution of the amide (Step 1) (5.0 g, 0.024 mole) in tetrahydrofuran (100 mL) was added t-butyl lithium (1.7M in pentane, 32.4 mL, 0.055 mole) dropwise. Dimethylformamide (2.3 mL, 0.03 mole) was added dropwise at −78° C. over 3 hours and the mixture allowed to warm room temperature. The reaction was quenched with ice water (200 mL) and extracted with ethyl acetate. The resulting organic phase was dried over MgSO4 and was concentrated in vacuo to a volume of 20 mL. A white solid precipitated which was collected by filtration yielding the formylated product (3.24 g, 56%): mp 168.7–170.8° C. 1H NMR (CDCl3/300 MHz) 10.60(br s, 1H), 9.88 (s, 1H), 8.57 (s, 1H), 8.00 (s, 1H), 1.28 (s, 9H). Anal. Calc'd for C11H13N2O2Cl: C, 54.89; H, 5.44; N, 11.64 Found: C, 54.87; H, 5.42; N, 11.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109211B2
Source datasetuspto-grants-2006_09
ORD IDord-df321a29e0d9494ca445d3526dd8d27d
Source noteuspto-grants-2006_09