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HRID 1427352作成日:2026年10月27日

Hydrochloric Acid → Ethyl 2-amino-3-oxo-3-(tetrahydrofuran-3-yl)propanoate, hydrochloride salt

https://huagongshe.com/reaction/1427352

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Lithium HexamethyldisilazideHCID 2733832—
反応物Tetrahydrofuran-3-carbonyl chlorideHCID 14020412—
反応物HCID 178472686HCID 178472686—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-amino-3-oxo-3-(tetrahydrofuran-3-yl)propanoate, hydrochloride saltHCID 131732346—

反応手順

Lithium bis(trimethysilyl)amide (1 M solution in tetrahydrofuran, 288 mL, 0.288 mol) was added drop-wise to a solution of ethyl (2E)-[(diphenylmethyl)imino]ethanoate (70 g, 0.26 mol) in tetrahydrofuran (1 L) at −70° C. The reaction mixture was stirred for 30 minutes, and the resulting suspension was transferred via cannula into a solution of tetrahydrofuran-3-carbonyl chloride (35.7 g, 0.26 mol) in tetrahydrofuran (200 mL) at −70° C. The reaction mixture was stirred at room temperature for 2 hours, at which time aqueous hydrochloric acid (2 M, 260 mL) was added. After the reaction mixture had stirred for 15 minutes, the tetrahydrofuran was removed in vacuo, and the aqueous residue was washed with ethyl acetate (4×200 mL). The aqueous layer was freeze-dried, affording the product as a light yellow solid. Yield: 40 g, 0.20 mol, 77%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08933224B2
出典データセットuspto-grants-2015_01
ORD IDord-5184103b253c454696c48cdd15f20b7b
出典メモuspto-grants-2015_01