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

Hydrochloric Acid → 3-Methoxynaphthalene-2-boronic acid

HRID 657182
노트
인쇄 미리보기

반응식

HRID 657182 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1.C([Li])CCC.[B:18](OC)([O:21]C)[O:19]C.Cl>O1CCCC1.C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[C:12]([B:18]([OH:21])[OH:19])=[CH:11][C:10]2[C:5]([CH:4]=1)=[CH:6][CH:7]=[CH:8][CH:9]=2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 71192-MethoxynaphthaleneHCID 8470Trimethyl borateHCID 178418339Butyllithium

생성물 1

HCID 108889523-Methoxynaphthalene-2-boronic acid수율 25.1%

시약·촉매·용매 2

HCID 6212Chloroform용매
HCID 8028
Tetrahydrofuran
용매

반응 조건

온도
0 °C

실험 절차

Under a nitrogen atmosphere, 15.0 g (94.9 mmol) of 2-methoxynaphthalene was dissolved in tetrahydrofuran (300 ml), and the solution was cooled to 0° C. After that, 238 mL (1.6-mol/L solution, 190 mmol) of normal butyllithium were slowly dropped to the solution. After the dropping, the mixture was stirred at 0° C. for 2 hours. After that, the mixture was cooled to −10° C., and 33 mL (340 mmol) of trimethyl borate was dropped over 10 minutes to the mixture. The resultant was heated to room temperature, and was stirred overnight. After that, 0.2N hydrochloric acid was added to the resultant to stop the reaction. Chloroform was added to the resultant to separate an organic layer, and the layer was washed with a saturated aqueous solution of ammonium chloride once and with water four times. After that, the solvent was removed by distillation, and heptane and toluene were added to the resultant residue to purify the residue by recrystallization, whereby 4.81 g of Intermediate Compound 6 were obtained.

후처리

  1. temperatureAfter that, the mixture was cooled to −10° C.
  2. temperatureThe resultant was heated to room temperature
  3. stirringwas stirred overnight
  4. customthe reaction
  5. customto separate an organic layer
  6. washthe layer was washed with a saturated aqueous solution of ammonium chloride once
  7. customAfter that, the solvent was removed by distillation, and heptane and toluene
  8. additionwere added to the resultant residue
  9. customto purify the residue
  10. customby recrystallization

출처 및 근거

ORD 기록
ord-13bce3e810154d09b9a219ae1fb2d8c5
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08072137B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트