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HRID 539349作成日:2026年10月27日

Hydrochloric Acid → 5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexan]-3-imine

https://huagongshe.com/reaction/539349

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Diethyl EtherHCID 3283—
反応物N-(5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamideHCID 67979520—
溶媒1,4-DioxaneHCID 31275—
生成物5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexan]-3-imineHCID 6797954491.4%

反応手順

To a solution of N-(5-bromo-4′-methoxy-3H-spiro[benzofuran-2,1′-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamide (Example 29 Step 1, 2 g, 4.83 mmol) in anhydrous 1,4-dioxane (40 mL) was added 4M HCl in 1,4-dioxane (12.07 mL, 48.27 mmol) and the resulting mixture was stirred under a nitrogen atmosphere at rt overnight. Et2O (30 mL) was added and the precipitate was filtered off and washed with Et2O, then partitioned between DCM (40 mL) and sat. aq. NaHCO3 (40 mL). The phases were separated and the organic layer concentrated, yielding 1.37 g of the crude title compound which was used immediately in the next step: MS (EI) m/z 309 M.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865911B2
出典データセットuspto-grants-2014_10
ORD IDord-74d2a0aed77d467c8553279954b76d1c
出典メモuspto-grants-2014_10