홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Triethylamine → Ethyl 3-aminobenzo[b]thiophene-2-carboxylate

HRID 1358277
노트
인쇄 미리보기

반응식

HRID 1358277 반응식
F[C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[CH3:10][CH2:11][O:12][C:13]([CH2:15][SH:16])=[O:14].CCN(CC)CC>CS(C)=O>[NH2:5][C:4]1[C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][C:2]=2[S:16][C:15]=1[C:13]([O:12][CH2:11][CH3:10])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 12185Ethyl ThioglycolateHCID 678552-Fluorobenzonitrile

생성물 1

HCID 731510Ethyl 3-aminobenzo[b]thiophene-2-carboxylate수율 70.5%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

2-Fluorobenzonitrile (0.61 g, 5 mmol), ethyl thioglycollate (0.60 g, 5 mmol) and NEt3 (1.52 g, 15 mmol) are stirred in DMSO (5 mL) at 100° C. under N2 for 3 h. The reaction mixture is poured onto ice-water (50 mL), and the solid is collected by suction filtration, rinsed with water, and air dried to give ethyl 3-aminobenzothiophene-2-carboxylate (0.78 g, 70%) as a grey-brown solid. 1H NMR (DMSO) δ8.14 (1H, d, J=7.7 Hz), 7.88 (1H, d, J=8.1 Hz), 7.50 (1H, dt, Jd=1.2 Hz, Jt=7.5 Hz), 7.39 (1H, dt, Jd=1.2 Hz, Jt=7.6 Hz), 7.17 (2H, brs), 4.26 (2H, q, J=7.1 Hz), 1.29 (3H, t, J=7.1 Hz).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionThe reaction mixture is poured onto ice-water (50 mL)
  2. filtrationthe solid is collected by suction filtration
  3. washrinsed with water, and air
  4. customdried

출처 및 근거

ORD 기록
ord-79082443edfe4b7ab3904767acbf15c5
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06596726B1

반응 노트

불러오는 중…