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

2-Naphthalenecarboxaldehyde → 2,2-Dimethyl-1-(2-naphthyl)-1,3-propanediol

HRID 29127
노트
인쇄 미리보기

반응식

HRID 29127 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]=[O:12].[OH-:13].[K+]>C(O)C>[CH3:1][C:2]([CH3:11])([CH2:3][OH:13])[CH:11]([C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:1]=1)[OH:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 62012-NaphthalenecarboxaldehydeHCID 14797Potassium Hydroxide

생성물 1

HCID 225011472,2-Dimethyl-1-(2-naphthyl)-1,3-propanediol수율 181.3%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

2-Naphthoaldehyde (26.0 g, 0.167 mol) and isobutylaldehyde (24.0 g, 0.33 mol) were dissolved in ethanol (50 ml) with heating. 85% Potassium hydroxide (11.0 g, 0.167 mol) dissolved in ethanol (150 ml) was added dropwise to the above solution with stirring. Exothermic reaction started immediately, and the temperature reached to 51° C. and then decreased. After the dropping was completed for about 10 min, the solution was stirred at 55 to 60° C. for 4 hr. The reaction solution was concentrated under reduced pressure, and water (150 ml) was added thereto and the mixture was extracted with chloroform (100 ml) twice. The extract was washed with saturated brine, dehydrated with anhydrous sodium sulfate and concentrated to give the title compound as a brown oil (34.86 g, yield 91.0%).

후처리

  1. temperaturewith heating
  2. additionwas added dropwise to the above solution
  3. customExothermic reaction
  4. customreached to 51° C.
  5. stirringthe solution was stirred at 55 to 60° C. for 4 hr
  6. concentrationThe reaction solution was concentrated under reduced pressure, and water (150 ml)
  7. additionwas added
  8. extractionthe mixture was extracted with chloroform (100 ml) twice
  9. washThe extract was washed with saturated brine
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f745ad5278f149238bdb5b3c84685fdd
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07420070B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트