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

Methyl 3-(4-(benzyloxy)phenyl)-3-oxopropanoate → Methyl (4-Hydroxybenzoyl)acetate

HRID 922324
노트
인쇄 미리보기

반응식

HRID 922324 반응식
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15](=[O:21])[CH2:16][C:17]([O:19][CH3:20])=[O:18])=[CH:11][CH:10]=1)C1C=CC=CC=1.[H][H]>[C].[Pd].C(OCC)(=O)C>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([C:15](=[O:21])[CH2:16][C:17]([O:19][CH3:20])=[O:18])=[CH:13][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 58806802Methyl 3-(4-(benzyloxy)phenyl)-3-oxopropanoateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 508465Methyl (4-Hydroxybenzoyl)acetate수율 98.1%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 8857Ethyl Acetate용매

실험 절차

To a 50 mL RB flask fitted with magnetic stirrer were charged ethyl acetate (15 mL), to that stirred solvent was added methyl 3-[4-(benzyloxy)phenyl]-3-oxopropanoate (0.3 g, 1.05 mmol), and palladium carbon 10% (80 mg) was added. After addition, the hydrogen balloon was fixed to the reaction mixture and stirred at room temperature for 1 h. After 3 h, the reaction mixture was filtered through celite. Then the organic layer was concentrated and dried. The product was obtained as colourless liquid (0.2 g, Yield: 98%).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customTo a 50 mL RB flask fitted with magnetic stirrer
  2. additionwas added
  3. additionAfter addition
  4. stirringstirred at room temperature for 1 h
  5. filtrationthe reaction mixture was filtered through celite
  6. concentrationThen the organic layer was concentrated
  7. customdried

출처 및 근거

ORD 기록
ord-22e8eafd66604a16adc4842b12db5e8e
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278915B2

반응 노트

불러오는 중…