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

Acetyl chloride → HCID 21955367, 화합물

HRID 2213042
노트
인쇄 미리보기

반응식

HRID 2213042 반응식
C(Cl)(=O)C.[CH2:5]1[C:10]2([CH2:15][CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][CH2:11]2)[CH2:9][CH2:8][CH2:7][O:6]1>CO>[CH2:5]1[C:10]2([CH2:11][CH2:12][NH:13][CH2:14][CH2:15]2)[CH2:9][CH2:8][CH2:7][O:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6367Acetyl chlorideHCID 21955183Tert-butyl 2-oxa-9-azaspiro[5.5]undecane-9-carboxylate

생성물 1

HCID 21955367HCID 21955367, 화합물수율 119.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Acetyl chloride (1 mL) was added to stirred, cooled (0° C.) methanol (10 mL) and the mixture was stirred at 0° C. for 5 minutes. 1,1-Dimethylethyl 2-oxa-9-azaspiro[5.5]undecane-9-carboxylate (Description 138, 78 mg, 0.27 mmol) was added and the mixture was stirred at room temperature for 3 hours. The solvent was evaporated under reduced pressure, aqueous sodium carbonate (10%, 10 mL) was added and the mixture was extracted with dichloromethane (3×10 mL). The combined organic fractions were dried (Na2SO4) and the solvent was evaporated under reduced pressure to give the title compound (50 mg, 100%). m/z (ES+) 156 (M+1).

후처리

  1. stirringthe mixture was stirred at 0° C. for 5 minutes
  2. stirringthe mixture was stirred at room temperature for 3 hours
  3. customThe solvent was evaporated under reduced pressure, aqueous sodium carbonate (10%, 10 mL)
  4. additionwas added
  5. extractionthe mixture was extracted with dichloromethane (3×10 mL)
  6. dry with materialThe combined organic fractions were dried (Na2SO4)
  7. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-814bd52efc5f4b43ba90b573fe34c479
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105507B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트