Réaction #607397

ord-b2cb491c33dc4ea98c04cf81bc925ef6

Équation de réaction

COC(=O)/C=C(C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C
solution
COC(=O)/C=C(C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C
(2Z,4E)-methyl 5-((S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoate
CI
methyl iodide
C[Si](C)(C)N[Si](C)(C)C.[Li]
Lithium hexamethyl disilazane
COC(=O)/C=C(C)\C=C\[C@@]1(O)C(C)=C(C)C(=O)CC1(C)C
title compound
COC(=O)/C=C(C)\C=C\[C@@]1(O)C(C)=C(C)C(=O)CC1(C)C
(2Z,4E)-methyl 5-((S)-1-hydroxy-2,3,6,6-tetramethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoate

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe ice bath was removed
  2. 2
    workup.STIRRINGThe resulting solution was stirred at ambient temperature overnight
  3. 3
    AutreThe reaction was quenched with saturated aqueous ammonium chloride solution (200 ml) and water (200 ml)
  4. 4
    Extractionextracted with ethyl acetate (3×150 ml)
  5. 5
    SéchageThe combined organic solution was dried (MgSO4)
  6. 6
    Filtrationfiltered
  7. 7
    Concentrationconcentrated
  8. 8
    AutreThe residue was purified on a silica gel column
  9. 9
    Lavageeluted with ethyl acetate and hexane

Mode opératoire

A solution of Example 1a (27.8 g, 0.1 mole) in anhydrous tetrahydrofuran (THF, 600 ml) was cooled to 0° C. with an ice bath under an atmosphere of nitrogen. Lithium hexamethyl disilazane (1.0 M solution in THF, 150 ml) was added dropwise via a syringe over about 30 minutes. The resulting solution was stirred at 0° C. for 30 minutes and the ice bath was removed. A solution of methyl iodide (8.09 ml, 18.4 g, 0.13 mole) in anhydrous THF (20 ml) was added via a syringe over 20 minutes. The resulting solution was stirred at ambient temperature overnight. The reaction was quenched with saturated aqueous ammonium chloride solution (200 ml) and water (200 ml) and extracted with ethyl acetate (3×150 ml). The combined organic solution was dried (MgSO4), filtered and concentrated. The residue was purified on a silica gel column eluted with ethyl acetate and hexane. The title compound was obtained as a white solid (17.1 g). 1HNMR (CDCl3): δ7.84 (d, 1H), 6.16 (d, 1H), 5.75 (s, 1H), 3.70 (s, 3H), 2.44 (d, 1H), 2.34 (d, 1H), 2.00 (s, 3H), 1.88 (s, 3H), 1.83 (s, 3H), 1.07 (s, 3H), 1.00 (s, 3H). MS (ESI—): m/e=291.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09326508B2uspto-grants-2016_05