Methanol → HCID 9886295, compound

HRID 1069210Notes

Reaction equation

HRID 1069210 reaction equation
[OH-].[K+].[Br:3][C:4]1[C:13]2[S:14][C:15]([CH3:18])=[C:16]([CH3:17])[C:12]=2[C:11]([C:19]2[CH:24]=[CH:23][C:22]([O:25]C(=O)C)=[CH:21][CH:20]=2)=[C:10]2[C:5]=1[CH:6]=[CH:7][CH:8]=[CH:9]2.CO>C1COCC1>[Br:3][C:4]1[C:13]2[S:14][C:15]([CH3:18])=[C:16]([CH3:17])[C:12]=2[C:11]([C:19]2[CH:20]=[CH:21][C:22]([OH:25])=[CH:23][CH:24]=2)=[C:10]2[C:5]=1[CH:6]=[CH:7][CH:8]=[CH:9]2

Participants

5

Reactant 3

HCID 887MethanolHCID 14797Potassium HydroxideHCID 12972353HCID 12972353, compound

Product 1

HCID 9886295HCID 9886295, compoundYield 73.2%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Aqueous potassium hydroxide (6.0 mL, 6.0 mmol) was added to a stirred, room temperature solution of acetic acid 4-(9-bromo-2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-phenyl ester (0.48 g, 1.14 mmol) in THF (15 mL)/methanol (10 mL). After 1 h, the organic solvents were removed, water was added, the reaction mixture was acidified with 10% HCl and the resulting solid was washed with water and triturated with pet. ether and then dried in vacuo to provide the title compound as a white solid (0.32 g, 73%): mp: 165-168° C.; NMR (DMSO-d6); δ9.68 (s, 1H), 8.17 (d, J=8 Hz, 1H), 7.62 (ddd, J=8, 6, 1 Hz, 1H), 7.50 (d, J=8 Hz, 1H), 7.44 (ddd, J=8, 7, 1 Hz, 1H), 7.13 (d, J=9 Hz, 2H), 6.91 (d, J=9 Hz, 2H), 2.42 (d, J=1 Hz, 3H), 1.59 (d, J=1 Hz, 3H); MS (EI): 1 bromine isotope pattern 382 (95%, MI), 384 (100%); Anal. Calc. for C20H15BrOS: C, 62.67; H, 3.95; N, 0.00. Found: C, 62.40; H, 3.91; N, 0.09.

Workup

  1. customthe organic solvents were removed
  2. additionwater was added
  3. washthe resulting solid was washed with water
  4. customtriturated with pet. ether
  5. customdried in vacuo

Sources & evidence

ORD record
ord-831d18fec6cf4f52a35627b2aff19f97
Source dataset
uspto-grants-2001_06
Patent number
US06251936B1

Reaction notes

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