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Boron trifluoride etherate → Tert-butyl 4-(adamantan-2-yl(hydroxy)methyl)-3-chlorobenzoate

HRID 1849749
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1849749
Br[C:2]1[CH:14]=[CH:13][C:5]([C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])=[CH:4][C:3]=1[Cl:15].[Cl-].[Li+].C([Mg]Cl)(C)C.[O:23]1[CH2:25][C:24]21[CH:32]1[CH2:33][CH:28]3[CH2:29][CH:30]([CH2:34][CH:26]2[CH2:27]3)[CH2:31]1.B(F)(F)F.CCOCC>O1CCCC1>[CH:26]12[CH2:34][CH:30]3[CH2:29][CH:28]([CH2:33][CH:32]([CH2:31]3)[CH:24]1[CH:25]([OH:23])[C:2]1[CH:14]=[CH:13][C:5]([C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])=[CH:4][C:3]=1[Cl:15])[CH2:27]2
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Komponenten

6

Edukt 4

HCID 8000Boron trifluoride etherateHCID 303804Spiro[adamantane-2,2'-oxirane]HCID 81295241Tert-butyl 4-bromo-3-chlorobenzoateHCID 178461733HCID 178461733, Verbindung

Produkt 1

HCID 86703631Tert-butyl 4-(adamantan-2-yl(hydroxy)methyl)-3-chlorobenzoateAusbeute 33 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a solution of tert-butyl 4-bromo-3-chlorobenzoate (0.875 g, 3.00 mmol) in tetrahydrofuran (5 mL) was added isopropylmagnesium chloride lithium chloride complex (1.3 M solution in anhydrous tetrahydrofuran, 2.78 mL, 3.61 mmol) at −40° C. The reaction was allowed to warm to ambient temperature and stirred for 1 hour (solution A). In a separate flask, a solution of spiro(adamantane-2,2′-oxirane) (0.492 g, 3.00 mmol) in anhydrous tetrahydrofuran (5 mL) was treated with boron trifluoride diethyl etherate (0.38 mL, 3.0 mmol) at 0° C. for 30 minutes (solution B). Solution A was then transferred via cannula to solution B at 0° C. The reaction mixture was allowed to warm to ambient temperature and stirred for 16 hours. After quenched with saturated ammonium chloride solution (5 mL), the mixture was extracted with ethyl acetate (3×10 mL). The combined organic phase was dried over anhydrous sodium sulfate, and filtered. Concentration of the filtrate in vacuo gave a residue which was purified by silica gel column chromatography using 0-100% ethyl acetate in hexanes as eluent to afford the title compound as a colorless solid (0.32 g, 33%): 1H NMR (300 MHz, DMSO-d6) δ 7.84 (dd, J=8.1, 1.4 Hz, 1H), 7.80 (d, J=1.5 Hz, 1H), 7.64 (d, J=8.1 Hz, 1H), 5.44 (br s, 1H), 5.18 (d, J=10.3 Hz, 1H), 2.36-2.29 (m, 1H), 2.06-1.34 (m, 22H), 1.08-1.01 (m, 1H); MS (ES+) m/z 359.2, 361.2 (M−17).

Aufarbeitung

  1. temperatureto warm to ambient temperature
  2. customAfter quenched with saturated ammonium chloride solution (5 mL)
  3. extractionthe mixture was extracted with ethyl acetate (3×10 mL)
  4. dry with materialThe combined organic phase was dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. customConcentration of the filtrate in vacuo gave a residue which
  7. customwas purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-914cc75b7c9c48459d2852ae63ddd59d
Quelldatensatz
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08952169B2

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