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

Catechol → 2-(Propan-2-yl)-2H-1,3-benzodioxole

HRID 1111595
노트
인쇄 미리보기

반응식

HRID 1111595 반응식
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].[CH:9](=O)[CH:10]([CH3:12])[CH3:11].O>C1C=CC=CC=1.S(=O)(=O)(O)O>[CH:10]([CH:12]1[O:4][C:3]2[CH:5]=[CH:6][CH:7]=[CH:8][C:1]=2[O:2]1)([CH3:11])[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 289CatecholHCID 962WaterHCID 6561Isobutyraldehyde

생성물 1

HCID 126081732-(Propan-2-yl)-2H-1,3-benzodioxole수율 33.5%

시약·촉매·용매 2

HCID 1118Sulfuric Acid촉매HCID 241Benzene용매

실험 절차

Catechol (22 g, 0.2 mole) and isobutyraldehyde (16 g, 0.24 mole) were dissolved in benzene (600 ml). A catalytic amount (5 drops) of sulfuric acid was added to the mixture. The mixture was heated under reflux and the water formed in the reaction was removed by use of a Dean-Stark trap. The reaction mixture was washed twice with aqueous sodium carbonate solution and dried. 2-Isopropyl-1,3-benzodioxole (11 g, 0.067 mole) was obtained by vacuum distillation. The 2-isopropyl-1,3-benzodioxole thus obtained boiled at 29-31° C. at 0.25 mm Hg. The nmr spectrum was consistent with the assigned structure.

후처리

  1. temperatureThe mixture was heated
  2. temperatureunder reflux
  3. customwas removed by use of a Dean-Stark trap
  4. washThe reaction mixture was washed twice with aqueous sodium carbonate solution
  5. customdried

출처 및 근거

ORD 기록
ord-26c49f2c2e3d476d9dd2aa105ca3079b
출처 데이터셋
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04118400

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트