3-Bromobiphenyl → methyl (2RS,4RS)-2-(3-phenylphenyl)-2,4-dimethyl-6-oxocyclohexanecarboxylate

温度

-90 °C

A solution of 3-bromobiphenyl (403 μL) in diethyl ether (4 mL) was stirred at −90° C. and treated slowly with n-butyllithium (1.6 M in hexanes, 1.5 mL). The resulting mixture was stirred at −90° C. for 20 min, and then transferred via a cannula to a stirred suspension of copper (I) cyanide (98 mg) in diethyl ether (1 mL) at −78° C. The mixture was stirred for 10 min at −78° C. and then warmed to 0° C. Once at the prescribed temperature, a solution of methyl 2,4-dimethyl-6-oxocyclohex-1-enecarboxylate (100 mg) in diethyl ether (1 mL) was added and the resulting mixture was warmed to rt over 30 min. Once at the prescribed temperature, the mixture was stirred at rt for 3 h. At the conclusion of this period, the mixture was treated with a 9:1 mixture of saturated aqueous ammonium chloride/ammonium hydroxide (10 mL). The resulting mixture was stirred for 10 min and then extracted three times with diethyl ether. The combined organic layers were washed with saturated aqueous ammonium chloride and saturated sodium chloride, dried over sodium sulfate and concentrated under vacuum to yield a residue. The residue was purified by chromatography on silica gel, eluting with 10% ethyl acetate/hexanes, to provide methyl (2RS,4RS)-2-(3-phenylphenyl)-2,4-dimethyl-6-oxocyclohexanecarboxylate (131.5 mg). Mass spectrum m/z 359.34 (M+Na+).

1. stirringThe mixture was stirred for 10 min at −78° C.
2. temperaturewarmed to 0° C
3. temperaturethe resulting mixture was warmed to rt over 30 min
4. stirringOnce at the prescribed temperature, the mixture was stirred at rt for 3 h
5. stirringThe resulting mixture was stirred for 10 min
6. extractionextracted three times with diethyl ether
7. washThe combined organic layers were washed with saturated aqueous ammonium chloride and saturated sodium chloride
8. dry with materialdried over sodium sulfate
9. concentrationconcentrated under vacuum
10. customto yield a residue
11. customThe residue was purified by chromatography on silica gel
12. washeluting with 10% ethyl acetate/hexanes

ORDレコード

ord-4011578800e6489ab1ab02eeca1c1980

出典データセット

uspto-grants-2013_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08507559B2