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

Hydrochloric Acid → 2-Iodo-5-(trifluoromethyl)phenol

HRID 1906518
노트
인쇄 미리보기

반응식

HRID 1906518 반응식
[H-].[Na+].[F:3][C:4]([F:13])([F:12])[C:5]1[CH:6]=[C:7]([OH:11])[CH:8]=[CH:9][CH:10]=1.[I:14]I.Cl>CCCCCC.C1(C)C=CC=CC=1.CCOCC>[I:14][C:8]1[CH:9]=[CH:10][C:5]([C:4]([F:12])([F:13])[F:3])=[CH:6][C:7]=1[OH:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 313Hydrochloric AcidHCID 807IodineHCID 73763-(Trifluoromethyl)phenolHCID 24758Sodium hydride2회

생성물 1

HCID 138235382-Iodo-5-(trifluoromethyl)phenol수율 102.1%

시약·촉매·용매 3

HCID 1140Toluene용매

실험 절차

To a round bottom flask under N2 was added 14.2 g (0.296 mole) of sodium hydride, 50% in oil. The NaH was washed twice with hexane, and 33.15 g (0.205 mole) of m-trifluoromethylphenol in 1 liter of toluene was added. After five minutes 51.9 g (0.205 mole) of iodine was added all at once, and the solution allowed to stir overnight. The reaction was poured into 3N HCl, ether added, and the separated organic layer washed with water, brine and dried with MgSo4. The solvent was evaporated in vacuo to give 60.3 g (100% yield) of 2-iodo-5-trifluoromethylphenol, mp 36°-38° C.

후처리

  1. additionwas added
  2. additionadded
  3. washthe separated organic layer washed with water, brine
  4. customdried with MgSo4
  5. customThe solvent was evaporated in vacuo

출처 및 근거

ORD 기록
ord-eb70b5ed65b748b3924dafad5bc5ddaf
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04652584

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 3283
Diethyl Ether
용매
HCID 8058Hexane용매