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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1278841생성일: 2026년 10월 27일

Ethylamine → Methyl 5-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-ylsulphonyl)penta-2,4-diynoate

https://huagongshe.com/reaction/1278841

반응식

참여 물질

역할이름HCID투입량
반응물EthylamineHCID 6341—
반응물Ammonium ChlorideHCID 25517—
반응물Methyl 3-bromoprop-2-ynoateHCID 294619—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물6-Ethynylsulphonyl-1,1,4,4,7-pentamethyl-1,2,3,4-tetrahydronaphthaleneHCID 22347825—
촉매Cuprous chlorideHCID 62652—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물Methyl 5-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-ylsulphonyl)penta-2,4-diynoateHCID 22347861—

반응 단계

A 70% solution of ethylamine in water (563 μl) is added dropwise to a mixture of methyl 3-bromopropynoate (632 mg, 2.88 mmol), hydroxylamine hydrochloride (162 mg, 2.33 mmol) and copper (I) chloride (10 mg) in methanol. A solution of 6-ethynylsulphonyl-1,1,4,4,7-pentamethyl-1,2,3,4-tetrahydronaphthalene (Example 7(b)) (500 mg, 1.94 mmol) in methanol (5 ml) is then added dropwise. The reaction medium is stirred for 15 h at room temperature and treated with saturated aqueous ammonium chloride solution and ethyl acetate. The organic phase is washed with water, dried over magnesium sulphate and concentrated. The product is obtained in the form of an oil after purification by flash chromatography on silica (80/20 heptane/CH2Cl2). 1H NMR/CDCl3: 1.26 to 1.28 (s, 12H); 1.67 (s, 4H); 2.35 (s, 3H); 3.78 (s, 3H); 7.14 (s, 1H); 7.48 (s, 1H); 13C NMR/CDCl3: 19.7; CH3/31.8; 4*CH3/34.1; Cq/34.3; Cq/34.9; 2*CH2/52.9; CH3/71.7; CH/72.1; CH/80.2; Cq/124.5; Cq/127.6; Cq/12.8.3; CH/129.3; CH/134.8; Cq/144.6; Cq/146.2; Cq/153.4; Cq.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06444709B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-0627d8b6b177464989eb15fb45861a70
출처 메모uspto-grants-2002_09