반응 #1473

ord-9be964bec0914ee8a55f4080f106b48c

반응 방정식

CC1(C)CCC(O[Si](C)(C)C(C)(C)C)c2cc(B(O)O)ccc21
(5,6,7,8-tetrahydro-5,5-dimethyl-8-(t-butyldimethylsilyloxy)naphth-2-yl)boronic acid
CCOC(=O)c1cccc2cc(Br)ccc12
ethyl 6-bromo-naphthalenecarboxylate
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Cc1ccccc1
toluene
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3O[Si](C)(C)C(C)(C)C)ccc2c1
title compound
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3O[Si](C)(C)C(C)(C)C)ccc2c1
Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-(t-butyldimethylsilyloxy)-naphth-7-yl]naphth-2-oate

용매

반응 조건

온도
90°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONThe reaction was diluted with 2N Na2 CO3
  2. 2
    추출extracted with CH2Cl2 (2×)
  3. 3
    세척the organic layer was washed with brine
  4. 4
    건조dried over MgSO4
  5. 5
    농축concentrated in vacuo
  6. 6
    기타to give an oil
  7. 7
    기타The crude product was purified flash chromatography (silica, 5% ethyl acetate in hexane)

실험 절차

To a degassed solution of 722 mg (2.6 mmol) of ethyl 6-bromo-naphthalenecarboxylate in 6.0 mL of toluene, was added sequentially 90 mg (0.08 mmol) of tetrakis-triphenylphosphine palladium (O), 5.0 mL (10.0 mmol) of 2M sodium carbonate, and a solution of 1.018 g (3.1 mmol) of (5,6,7,8-tetrahydro-5,5-dimethyl-8-(t-butyldimethylsilyloxy)naphth-2-yl)boronic acid (Compound B14) in 3.0 mL of MeOH. The reaction was heated at 90° C. for 15 h. The reaction was diluted with 2N Na2 CO3, and extracted with CH2Cl2 (2×), the organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. The crude product was purified flash chromatography (silica, 5% ethyl acetate in hexane) to afford the title compound as a white solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723666uspto-grants-1998_03