Lithium Hydroxide → HCID 57864405, compound

HRID 1672656Notes

Reaction equation

HRID 1672656 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:12][CH2:13][C:14]#[C:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=2)=[C:6]([CH:11]=1)[C:7]([O:9]C)=[O:8].[OH-].[Li+]>CO.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:12][CH2:13][C:14]#[C:15][C:16]2[CH:17]=[CH:18][C:19]([C:22]([F:23])([F:24])[F:25])=[CH:20][CH:21]=2)=[C:6]([CH:11]=1)[C:7]([OH:9])=[O:8]

Participants

5

Procedure

100 mg (0.28 mmol) of methyl 5-fluoro-2-[3-(4-trifluoromethylphenyl)prop-2-ynyloxy]benzoate are dissolved in 2 ml of methanol and 2 ml of water, and 20.3 mg (0.85 mmol) of lithium hydroxide are added. After stirring at room temperature for 12 h, the crystals which have separated out are filtered off with suction, washed with water, 1 N hydrochloric acid and petroleum ether and dried on a clay dish. 74.9 mg (0.20 mmol, 71% of theory) of the title compound are isolated.

Workup

  1. customthe crystals which have separated out
  2. filtrationare filtered off with suction
  3. washwashed with water, 1 N hydrochloric acid and petroleum ether
  4. customdried on a clay dish

Sources & evidence

ORD record
ord-8fd656b0586d435e9e4aa209aac90977
Source dataset
uspto-grants-2011_08
Patent number
US07998988B2

Reaction notes

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