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Pinacol → 2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

HRID 39604
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HRID 39604 반응식
[B:1]([O:10][CH:11]([CH3:13])[CH3:12])([O:6][CH:7]([CH3:9])[CH3:8])OC(C)C.[Cl:14][CH2:15]I.C([Li])CCC.Cl.C(OCC)(=O)C.OC(C(O)(C)C)(C)C>CCCCCC.O1CCCC1>[Cl:14][CH2:15][B:1]1[O:6][C:7]([CH3:8])([CH3:9])[C:11]([CH3:12])([CH3:13])[O:10]1
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참가 물질

8

반응물 5

HCID 6425PinacolHCID 11644ChloroiodomethaneHCID 21531Triisopropyl borateHCID 21866389Hydrogen chloride-ethyl acetateHCID 178418339Butyllithium

생성물 1

HCID 111268102-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane수율 81%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매
HCID 8058Hexane용매

실험 절차

To the mixture of triisopropyl borate (15 ml, 65 mmol), chloroiodomethane (13 g, 72 mmol), and tetrahydrofuran (78 ml), n-butyllithium (a 1.6 M n-hexane solution, 41 ml, 65 mmol) was added dropwise at −78° C. (an outer temperature) for 20 min, and then the obtained mixture was stirred at room temperature for 2.5 hours. The reaction mixture was cooled to 0° C. (an outer temperature), and a 4 N hydrochloric acid-ethyl acetate solution was added dropwise thereto at the same temperature until the reaction mixture became neutral. At the same temperature, pinacol (7.7 g, 65 mmol) was added to the reaction mixture, and then the reaction mixture was stirred at room temperature for 40 min. The solvents were evaporated under reduced pressure, and then the obtained residue was distilled under reduced pressure (63-70° C., 11 mmHg), thereby obtaining the entitled compound (9.2 g, 52 mmol, 81%).

후처리

  1. additionwas added dropwise at −78° C. (an outer temperature) for 20 min
  2. additionwas added dropwise
  3. stirringthe reaction mixture was stirred at room temperature for 40 min
  4. customThe solvents were evaporated under reduced pressure
  5. distillationthe obtained residue was distilled under reduced pressure (63-70° C., 11 mmHg)

출처 및 근거

ORD 기록
ord-9a7a9e92b21340fe8e2bf03088ad2df9
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524946B2

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