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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680531Generated: November 2, 2026

Iodoethane → HCID 178474098, compound

https://huagongshe.com/reaction/1680531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178469477HCID 178469477—
SolventDimethylformamideHCID 6228—
ProductHCID 178474098HCID 17847409872.5%

Reaction Conditions

Temperature95 °C

Reaction Steps

4-Hydroxy-5-hydroxyimino-5,6,7,8-tetrahydroquinoline-3-carboxylic acid ethyl ester (3.75 g) was suspended in 100 ml of dimethylformamide and then dissolved therein by stirring the suspension on an oil bath at 95° C. Thereafter, 1.04 g of potassium carbonate and then 2.32 g of ethyl iodide were added thereto. The resulting reaction mixture was stirred for 4 hours. After the dimethylformamide was distilled off under reduced pressure, water and ethyl acetate were added to the residue. The organic layer was separated and then stripped of solvent to obtain a yield of 3.0 g of the desired compound. This compound melted at 89°-91° C. (uncorrected values). Its infrared absorption spectrum (KBr tablet) had absorption peaks at 3440, 3000, 2960, 1740, 1640, 1465, 1220, 1190, 1110, 1060, and 990 cm-1, and its n.m.r. spectrum (CDCl3, 60Mc, TMS) had signals at δ values of 1.38 (3H, t, J=6.75 Hz), 1.42 (3H, t, J=7.5 HZ), 1.7-2.2 (2H, m), 2.7-3.15 (4H , m), 4.25 (2H, q. J=6.75 Hz), 4.40 (2H, q, J=7.5 Hz), and 8.77 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04273932
Source datasetuspto-grants-1981_06
ORD IDord-d35a3f8d16a9474c83d062745f15b2c9
Source noteuspto-grants-1981_06