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

2-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)thiazole → 2-(1,4-Dioxa-spiro[4.5]dec-8-yl)-thiazole

HRID 1173251
노트
인쇄 미리보기

반응식

HRID 1173251 반응식
[O:1]1[C:5]2([CH2:10][CH2:9][C:8]([C:11]3[S:12][CH:13]=[CH:14][N:15]=3)=[CH:7][CH2:6]2)[O:4][CH2:3][CH2:2]1>CO.[Pd]>[O:4]1[C:5]2([CH2:10][CH2:9][CH:8]([C:11]3[S:12][CH:13]=[CH:14][N:15]=3)[CH2:7][CH2:6]2)[O:1][CH2:2][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 595561422-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)thiazole

생성물 1

HCID 595560502-(1,4-Dioxa-spiro[4.5]dec-8-yl)-thiazole수율 95%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a Parr hydrogenation bottle was added 2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-1,3-thiazole (0.22 g, 0.99 mmol), dissolved in methanol (15 mL), followed by the addition of 10% Pd/C (0.08 g). This mixture was hydrogenated at 50 psi overnight. After the catalyst was filtered and washed with methanol, the filtrate was concentrated in vacuo to give 0.21 g of 2-(1,4-dioxaspiro[4.5]dec-8-yl)-1,3-thiazole in 95% yield. MS (EI) calcd: (M+1)+=226.1; found: 225.9.

후처리

  1. customwas hydrogenated at 50 psi overnight
  2. filtrationAfter the catalyst was filtered
  3. washwashed with methanol
  4. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-1e28fca03fb14477bc191932462d0cf5
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07834021B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트