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

Phosphinic Acid → 2-tert-Butyl-6-((2-methoxybiphenyl-3-yl)(phenyl)methyl)phenol

HRID 1042520
노트
인쇄 미리보기

반응식

HRID 1042520 반응식
C([O:8][C:9]1[C:14]([C:15]([CH3:18])([CH3:17])[CH3:16])=[CH:13][CH:12]=[CH:11][C:10]=1[C:19]([C:27]1[C:28]([O:39][CH3:40])=[C:29]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH:30]=[CH:31][CH:32]=1)([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)O)C1C=CC=CC=1.[PH2](O)=O>C(#N)C>[C:15]([C:14]1[CH:13]=[CH:12][CH:11]=[C:10]([CH:19]([C:27]2[C:28]([O:39][CH3:40])=[C:29]([C:33]3[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=3)[CH:30]=[CH:31][CH:32]=2)[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:9]=1[OH:8])([CH3:18])([CH3:16])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4124402Phosphinic AcidHCID 58238509(2-(Benzyloxy)-3-tert-butylphenyl)(2-methoxybiphenyl-3-yl)(phenyl)methanol

생성물 1

HCID 582385182-tert-Butyl-6-((2-methoxybiphenyl-3-yl)(phenyl)methyl)phenol수율 85%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A solution of 15 (1.02 g, 1.93 mmol) in acetonitrile (24 mL) was treated with 50% aqueous hypophosphorous acid (11 mL) and stirred at reflux for 1.5 hr. After cooling, the acetonitrile was removed on a rotary evaporator. The residue was diluted with water (100 mL) and extracted with ethyl acetate (150 mL). The organic layer was washed with water (100 mL), saturated sodium bicarbonate (100 mL) and water (100 mL). The organic layer was dried over sodium sulfate and stripped. The crude product was purified by chromatography on silica (60 g) with 1% ethyl acetate in hexane (2 L). The relevant fractions were stripped and the residue was taken up in ethanol (12 mL) and stirred at 60° C. on a water bath for 30 min. The resulting slurry was allowed to cool overnight. The crystals were collected by filtration, washed with cold ethanol and dried in a vacuum oven at 65° C. to produce pure B4 (0.69 g, 85%).

후처리

  1. temperatureat reflux for 1.5 hr
  2. temperatureAfter cooling
  3. customthe acetonitrile was removed on a rotary evaporator
  4. additionThe residue was diluted with water (100 mL)
  5. extractionextracted with ethyl acetate (150 mL)
  6. washThe organic layer was washed with water (100 mL), saturated sodium bicarbonate (100 mL) and water (100 mL)
  7. dry with materialThe organic layer was dried over sodium sulfate
  8. customThe crude product was purified by chromatography on silica (60 g) with 1% ethyl acetate in hexane (2 L)
  9. stirringstirred at 60° C. on a water bath for 30 min
  10. temperatureto cool overnight
  11. filtrationThe crystals were collected by filtration
  12. washwashed with cold ethanol
  13. customdried in a vacuum oven at 65° C.

출처 및 근거

ORD 기록
ord-d2f5cab5ffec41298694799aa1e18f8a
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557936B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트