Toluene → HCID 70872198, compound

HRID 1475754Notes

Reaction equation

HRID 1475754 reaction equation
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[C:6](Br)[CH:5]=1.[F:14][C:15]1[CH:16]=[C:17](B(O)O)[CH:18]=[CH:19][C:20]=1[O:21][CH3:22].C(=O)(O)[O-].[Na+].C1(C)C=CC=CC=1>[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>[CH3:1][O:2][C:3]([C:4]1[CH:5]=[C:6]([C:17]2[CH:18]=[CH:19][C:20]([O:21][CH3:22])=[C:15]([F:14])[CH:16]=2)[C:7]([O:10][CH3:11])=[CH:8][CH:9]=1)=[O:13]

Participants

7

Procedure

3-Bromo-4-methoxybenzoic acid methyl ester (500 mg, 2.04 mmol), 3-fluoro-4-methoxyphenylboronic acid (381 mg, 2.24 mmol), Tetrakis(triphenylphosphine)-palladium(0) (117 mmol, 0.10 mmol), and sodium bicarbonate (514 mg, 6.12 mmol) were partitioned between toluene (5 ml) and water (5 ml) and stirred in reflux for 36 hours. The mixture was partitioned between ethyl acetate and water, the combined organic extracts were dried over sodium sulfate and evaporated to dryness. The raw material was purified by silica gel chromatography with a heptane/ethyl acetate gradient. to yield the title compound (500 mg).

Workup

  1. temperaturein reflux for 36 hours
  2. customThe mixture was partitioned between ethyl acetate and water
  3. dry with materialthe combined organic extracts were dried over sodium sulfate
  4. customevaporated to dryness
  5. customThe raw material was purified by silica gel chromatography with a heptane/ethyl acetate gradient

Sources & evidence

ORD record
ord-0de7f2f47d864ffe9c7225c88887b3ff
Source dataset
uspto-grants-2015_04
Patent number
US09018383B2

Reaction notes

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