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HRID 12507作成日:2026年10月26日

Hydrochloric Acid → [4-(Aminomethyl)oxan-4-yl]methanamine

https://huagongshe.com/reaction/12507

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Sodium HydroxideHCID 14798—
反応物Borane;tetrahydrofuranHCID 2723981—
反応物Dihydro-2H-pyran-4,4(3H)-dicarbonitrileHCID 14537194—
溶媒TetrahydrofuranHCID 8028—
生成物[4-(Aminomethyl)oxan-4-yl]methanamineHCID 6873862.1%

反応条件

温度-10 °C

反応手順

Tetrahydro-pyran-4,4-dicarbonitrile (1.52 g) was dissolved in dry THF (25 mL) and cooled to −10° C. To this solution, BH3.THF (56 mL of an 1M solution in THF, 5 equiv.) was added dropwise, the mixture was allowed to warm to room temperature, and subsequently stirred at 60° C. for 6 h. The mixture was cooled in an ice bath, and HCl (24.2 mL of a 6M aqueous solution, 13 equiv.) was added. The mixture was allowed to warm to room temperature and stirred for 2 h. The mixture was neutralized with 2M aqueous NaOH and extracted three times with DCM. The aqueous layer was evaporated to dryness, the residue was stirred with CHCl3, the solids were filtered off and the organic phase was evaporated under reduced pressure to yield 1.0 g (62%) of a yellow oil. 1H NMR (400 MHz, CDCl3) δ 1.46 (t, 4H), 2.74 (s, 4H), 3.67 (t, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728018B2
出典データセットuspto-grants-2010_06
ORD IDord-b024ed43abc34f699c2cabd633dfb5f9
出典メモuspto-grants-2010_06