1-Naphthol → 1-(2-Bromoethoxy)naphthalene

HRID 615618

반응식

HRID 615618 반응식
[C:1]1([OH:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[OH-].[K+].C1(C([O-])=O)C2C(=CC=CC=2)C=CC=1.[K+].[Br:28][CH2:29][CH2:30]Br>C(O)C>[Br:28][CH2:29][CH2:30][O:11][C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

참가 물질

6

반응물 4

HCID 70051-NaphtholHCID 78391,2-DibromoethaneHCID 14797Potassium HydroxideHCID 23664128Potassium naphthalate

생성물 1

HCID 110759061-(2-Bromoethoxy)naphthalene수율 50.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 144.0 g (1 mole) α-naphthol and 56.1 g (1 mole) potassium hydroxide in 600 ml of 95% ethanol was stirred 1.5 hr at room temperature. To this solution of potassium naphthalate was added 930.0 g (5.0 mole) of 1,2-dibromoethane, and the solution was heated at reflux overnight. The reaction mixture was filtered, and the filtrate stripped to dryness under reduced pressure in a rotary evaporator. The resulting oil was dissolved in chloroform and the solution extracted with 10% aqueous sodium hydroxide. The chloroform layer was dried and stripped of chloroform to yield 126 g (50.3%) of dark brown oil.

후처리

  1. temperaturethe solution was heated
  2. temperatureat reflux overnight
  3. filtrationThe reaction mixture was filtered
  4. customthe filtrate stripped to dryness under reduced pressure in a rotary evaporator
  5. dissolutionThe resulting oil was dissolved in chloroform
  6. extractionthe solution extracted with 10% aqueous sodium hydroxide
  7. dry with materialThe chloroform layer was dried

출처 및 근거

ORD 기록
ord-e126e237c225482f838909074476a55e
출처 데이터셋
uspto-grants-1985_02
특허 번호
US04500529

연결된 노트

불러오는 중…