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HRID 480356作成日:2026年10月25日

Hydrochloric Acid → 5-(Methanesulfonylamino-methyl)-thiophen-2-yl-acetic acid methyl ester

https://huagongshe.com/reaction/480356

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FormaldehydeHCID 712—
反応物MethanesulfonamideHCID 72879—
反応物Methyl thiophen-2-acetateHCID 88055—
触媒ZincchlorideHCID 3007855—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物5-(Methanesulfonylamino-methyl)-thiophen-2-yl-acetic acid methyl esterHCID 5445733669%

反応手順

To a solution of thiophen-2-yl-acetic acid methyl ester (2 mL, 12.8 mmol) in 1,4-dioxane (10 mL) was added concentrated HCl (0.4 mL, 4.8 mmol) dropwise over 10 minutes. Zinc chloride (78 mg, 0.57 mmol) was added and the reaction was lowered into a pre-heated water bath at 45° C. and was stirred for 15 minutes. HCl (g) was bubbled into the solution for 2-3 minutes. The temperature of the reaction rose to about 60° C. Upon cooling, 37% aqueous formaldehyde (1.24 mL, 16 mmol) was added dropwise and the temperature rose to 70° C. The reaction was cooled to room temperature and methanesulfonamide (1.25 g, 12.8 mmol) was added in portions. The reaction was stirred for 3 h and was poured into EtOAc (60 mL). The organic solution was washed with water and the aqueous solution was washed with EtOAc (60 mL). The combined organic solutions were washed with brine, dried over MgSO4, filtered, and concentrated. Purification by flash chromatography (CHCl3) provided the title compound (69%) as a gold oil. 1H NMR (400 MHz, CDCl3) δ 6.85 (d, 1H), 6.70 (d, 1H), 5.20 (m, 1H), 4.40 (s, 2H), 3.80 (s, 2H), 3.70 (s, 3H), 2.80 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06649657B2
出典データセットuspto-grants-2003_11
ORD IDord-eb773b7909af47c79e06264d7212ea21
出典メモuspto-grants-2003_11