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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601167생성일: 2026년 10월 23일

Methyl cyanoacetate → Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylate

https://huagongshe.com/ko/reaction/601167

반응식

참여 물질

역할이름HCID투입량
반응물Methyl cyanoacetateHCID 7747—
반응물TriethylamineHCID 8471—
반응물2-Propanone, 1-(acetyloxy)-3-chloro-HCID 38413—
반응물Sodium sulfide nonahydrateHCID 73972—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylateHCID 1588979051%

반응 단계

A solution of methyl cyanoacetate (1.18 mL, 13.28 mmol) and sodium sulfide nonahydrate (3.20 g, 13.28 mmol) in methanol (25 mL) at 0° C. was treated with 1-acetoxy-3-chloroacetone (2.0 g, 13.28 mmol). The cold bath was removed and triethylamine (1.86 mL, 13.28 mmol) was added dropwise. The solution was stirred at room temperature for 20 hours then diluted with water and extracted into ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and the solvent removed under vacuum to provide the titled compound (1.25 g, 51%). MS (DCI/NH3) M/Z 188 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 3.68 (s, 3 H) 4.45 (dd, J=5.52, 1.47 Hz, 2 H) 4.88 (t, J=5.70 Hz, 1 H) 6.12 (s, 1 H) 7.28 (s, 2 H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902203B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-34d3693602e0460bb323e90f52a7b8b0
출처 메모uspto-grants-2011_03