돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480356생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/480356

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물MethanesulfonamideHCID 72879—
반응물Methyl thiophen-2-acetateHCID 88055—
촉매ZincchlorideHCID 3007855—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물5-(Methanesulfonylamino-methyl)-thiophen-2-yl-acetic acid methyl esterHCID 5445733669%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649657B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-eb773b7909af47c79e06264d7212ea21
출처 메모uspto-grants-2003_11