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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358155Generated: October 31, 2026

Isoamyl Nitrite → HCID 86759068, compound

https://huagongshe.com/reaction/1358155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 18183644HCID 18183644—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86759068HCID 86759068—

Reaction Steps

11.0 g (0.206 mol) of sodium methoxide is suspended in 130 ml of methanol. Then isoamyl nitrite (27 ml, 0.206 mol) and 25 g (0.129 mol) of 1-(4-Methylsulfanyl-phenyl)-butan-1-one dissolved in 70 ml of tetrahydrofuran (THF) are added and the reaction solution is stirred at room temperature for 1.5 days. After concentrating, water and acetic acid are added to neutralise. The crude product is extracted with ethyl acetate, washed with brine, dried over MgSO4, and concentrated. The residue is purified by column chromatography on silica gel with ethyl acetate-hexane (15:85) as an eluent. The structure is confirmed by the 1H-NMR spectrum (CDCl3). δ[ppm]: 1.14 (t, 3H), 2.52 (s, 3H), 2.72 (q, 2H), 7.25 (d, 2H), 7.89 (d, 2H), 8.01 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596445B1
Source datasetuspto-grants-2003_07
ORD IDord-5b0f4e6c4cc74a878aaa9d4939dae047
Source noteuspto-grants-2003_07