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

Water → 3,3-Dimethyl-2,3-dihydro-1-benzofuran-4-ol

HRID 1484627
노트
인쇄 미리보기

반응식

HRID 1484627 반응식
[CH3:1][C:2]1([CH3:13])[C:6]2[C:7]([O:11]C)=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH2:3]1.B(Br)(Br)Br.O>ClCCl>[CH3:1][C:2]1([CH3:13])[C:6]2=[C:7]([OH:11])[CH:8]=[CH:9][CH:10]=[C:5]2[O:4][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 575170913,3-Dimethyl-4-(methyloxy)-2,3-dihydro-1-benzofuran2회

생성물 1

HCID 574112993,3-Dimethyl-2,3-dihydro-1-benzofuran-4-ol수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 3,3-dimethyl-4-(methyloxy)-2,3-dihydro-1-benzofuran (Intermediate 5, 4.0 g) in dichloromethane (100 ml, SCRC) was added BBr3 (6.37 ml, 67.3 mmol, SCRC) dropwise under ice-cooling. After the addition was complete, the reaction mixture was stirred for 2 hours at room temperature and then water (20 ml) was added. The resulting mixture was extracted with ethyl acetate (3 times 100 ml, SCRC) and the combined organic layers were dried, evaporated and purified by silica gel chromatography with EtOAc/PE as eluents (1/20) to afford the title compound (2.8 g).

후처리

  1. temperaturecooling
  2. additionAfter the addition
  3. extractionThe resulting mixture was extracted with ethyl acetate (3 times 100 ml, SCRC)
  4. customthe combined organic layers were dried
  5. customevaporated
  6. custompurified by silica gel chromatography with EtOAc/PE as eluents (1/20)

출처 및 근거

ORD 기록
ord-79e6b209ee4e414cb5e97960e6115d46
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422272B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트