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

1,4-Dibromobutane → 3-[(4-Bromobutoxy)methyl]-3-ethyloxetane

HRID 7329
노트
인쇄 미리보기

반응식

HRID 7329 반응식
[OH:1][CH2:2][C:3]1([CH2:7][CH3:8])[CH2:6][O:5][CH2:4]1.[Br:9][CH2:10][CH2:11][CH2:12][CH2:13]Br.CCCCCC.[OH-].[Na+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[Br:9][CH2:10][CH2:11][CH2:12][CH2:13][O:1][CH2:2][C:3]1([CH2:7][CH3:8])[CH2:6][O:5][CH2:4]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 80561,4-DibromobutaneHCID 8058HexaneHCID 14798Sodium HydroxideHCID 76444Oxt-101

생성물 1

HCID 219893153-[(4-Bromobutoxy)methyl]-3-ethyloxetane수율 45%

시약·촉매·용매 2

HCID 74236Tetrabutylammonium Bromide촉매
HCID 962
Water
용매

반응 조건

온도
80 °C

실험 절차

Into a 2 L egg plant type flask were charged 46.3 g (0.40 mol) of 3-hydroxymethyl-3-ethyloxetane (product name: OXT-101 manufactured by Toagosei Co., Ltd.), 250.3 g (1.16 mol) of 1,4-dibromobutane (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.), and 275 ml of hexane. 500 ml of a 33% sodium hydroxide aqueous solution containing 2 g of tetra-n-butylammonium bromide (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added to the mixture and vigorously stirred for 5 hours. After the mixture was refluxed at a temperature of 80° C. for one hour, 500 ml of deionized water was added thereto so as to separate the mixture into an organic phase and an aqueous phase. The aqueous phase was extracted three times with 160 ml of hexane. After the organic phase and the extracted phase were dried over magnesium sulfate, the solvent was distilled out in a vacuum. The resulting transparent liquid was distilled in a vacuum thereby obtaining 44.5 g (0.18 mol) of 3-[(4-bromobutoxy)methyl]-3-ethyloxetane as a distillate at 109° C./532 Pa (yield: 44%, identified with 1H-NMR).

후처리

  1. additionwas added to the mixture
  2. customso as to separate the mixture into an organic phase
  3. extractionThe aqueous phase was extracted three times with 160 ml of hexane
  4. dry with materialAfter the organic phase and the extracted phase were dried over magnesium sulfate
  5. distillationthe solvent was distilled out in a vacuum
  6. distillationThe resulting transparent liquid was distilled in a vacuum

출처 및 근거

ORD 기록
ord-9bdd41d1c9294f7b851c289c0070b4ce
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07087273B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트