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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42271Generated: October 26, 2026

Diiodomethane → HCID 178469927, compound

https://huagongshe.com/reaction/42271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 178469928HCID 178469928—
ProductHCID 178469927HCID 178469927—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A mixture of ethyl 3-amino-pyrazole-4-carboxylate (6.4 g, 40 mmole) and diiodomethane (200 g) was cooled to −10° C. Isoamyl nitrite (24 mL, 180 mmole) was added via a syringe over 30 minutes. The mixture was allowed to warm up to ambient temperature and then stirred at 100° C. for 2 hours. After cooling to room temperature, the mixture was concentrated and the residue was dissolved in ethyl acetate (200 mL) and washed with 0.5 M aqueous sodium metasulfite solution (2×70 mL), 1 N HCl and brine. The organic solution was dried with magnesium sulfate and concentrated. The crude product was purified on a silica gel column eluting with 15% ethyl acetate in hexane to provide the title compound. MS (DCI) m/e 266.9 (M+H)+, 283.9 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536180B2
Source datasetuspto-grants-2013_09
ORD IDord-1512374cf2614d89bf62f46371ac9072
Source noteuspto-grants-2013_09