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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546296Generated: October 30, 2026

Thionyl Chloride → HCID 58598870, compound

https://huagongshe.com/reaction/546296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 3729139HCID 3729139—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58598870HCID 58598870—

Reaction Steps

Thionyl chloride (1.9 mL, 26.4 mmol) was added to a solution of 2,2a,7,7a-tetrahydro-cyclobuta[a]inden-1-one oxime (1.5 g, 8.8 mmol) in 1,4-dioxane (44 mL), and stirred overnight at room temperature. The reaction was quenched with saturated aqueous NaHCO3 (100 mL), and extracted with EtOAc (3×50 mL). The organic extracts were washed with brine, dried over MgSO4, and concentrated to give the subtitle compound and its regioisomer, which were used without further purification. MS calculated for C11H11NO+H: 174, observed: 174.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935830B2
Source datasetuspto-grants-2011_05
ORD IDord-cf48661b97354fa99b74da04b887814d
Source noteuspto-grants-2011_05