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

Acetone → HCID 15165618, 화합물

HRID 704008
노트
인쇄 미리보기

반응식

HRID 704008 반응식
[CH2:1]([C:5]1[CH:6]=[C:7]([OH:12])[C:8](=[CH:10][CH:11]=1)[OH:9])[CH:2]([CH3:4])[CH3:3].[CH3:13][C:14]([CH3:16])=O.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH2:1]([C:5]1[CH:11]=[CH:10][C:8]2[O:9][C:14]([CH3:16])([CH3:13])[O:12][C:7]=2[CH:6]=1)[CH:2]([CH3:4])[CH3:3]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180AcetoneHCID 521998p-Toluenesulfonic acid monohydrateHCID 143726654-(2-Methylpropyl)-1,2-benzenediol

생성물 1

HCID 15165618HCID 15165618, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

The same procedures as described in Example 10 were carried out by using 4.16 g (25 mM) of 4-isobutylcatechol, 15 ml of acetone, 30 mg of p-toluenesulfonic acid monohydrate and 15 ml of toluene. 5-Isobutyl-2,2-dimethyl-1,3-benzodioxol was obtained in the yield of 4.69 g (23 mM) as colorless transparent liquid having a boiling point of 79°-83° C./2 mmHg.

출처 및 근거

ORD 기록
ord-3d52b60b84634b9dbf0d80c7750c40d2
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04985458

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트