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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926625Generated: November 2, 2026

Diiodomethane → HCID 59250036, compound

https://huagongshe.com/reaction/1926625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 59250010HCID 59250010—
SolventAcetonitrileHCID 6342—
ProductHCID 59250036HCID 5925003637.2%

Reaction Conditions

Temperature38 °C

Reaction Steps

To a suspension of ethyl 5-amino-4-cyano-3-(2,4-dichlorophenyl)thiophene-2-carboxylate (2.92 g, 0.00856 mol) in acetonitrile (10 mL) was added diiodomethane (2.41 mL, 0.0300 mol) under an atmosphere of argon and was heated at 38° C. Isoamyl nitrite (2.61 g, 0.0214 mol) was added dropwise and the reaction mixture was cooled to room temperature and stirred for one hour. The reaction was concentrated in vacuo and column chromatography was performed to yield the title compound (1.44 g, 37%) as an orange solid. 1H NMR (400 MHz, d1-chloroform) δ: 7.53 (d, 1H, J=2.00 Hz), 7.38-7.34 (m, 1H), 7.21 (d, 1H, J=8.28 Hz), 4.25-4.15 (m, 2H), 1.21-1.16 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183240B2
Source datasetuspto-grants-2012_05
ORD IDord-eedb09bbae8446e6aae87cc52cbc8030
Source noteuspto-grants-2012_05