Thiourea → HCID 22648874, compound

HRID 393283Notes

Reaction equation

HRID 393283 reaction equation
[NH2:1][C:2]([NH2:4])=[S:3].Br[CH2:6][C:7]([C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[C:11]([CH3:16])[CH:10]=1)=O>O1CCOCC1>[NH2:1][C:2]1[S:3][CH:6]=[C:7]([C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[C:11]([CH3:16])[CH:10]=2)[N:4]=1

Participants

4

Conditions

Temperature
25 °C

Procedure

Thiourea (79.8 mg, 1.05 mmol) was added to a solution of 2-bromo-1-(4-hydroxy-3-methylphenyl)ethanone (200 mg, 0.87 mmol) in 1,4-dioxane (15 mL). The reaction mixture was stirred at 25° C. for 24 h. The resulting suspension was filtered and the solid was washed with 1,4-dioxane and dried under reduced pressure. The solid was suspended in water (30 mL), pH 7 buffer solution (15 mL) was added and the mixture was extracted with EtOAc (3×50 mL). The combined organic layers were successively washed with water (20 mL) and brine (20 mL), dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (Hexane:EtOAc, 1:1) to give the title compound (180 mg, 100% yield).

Workup

  1. filtrationThe resulting suspension was filtered
  2. washthe solid was washed with 1,4-dioxane
  3. customdried under reduced pressure
  4. additionpH 7 buffer solution (15 mL) was added
  5. extractionthe mixture was extracted with EtOAc (3×50 mL)
  6. washThe combined organic layers were successively washed with water (20 mL) and brine (20 mL)
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by flash chromatography (Hexane:EtOAc, 1:1)

Sources & evidence

ORD record
ord-96fcdb23cd8d45479baa46c5247ac730
Source dataset
uspto-grants-2004_10
Patent number
US06806265B2

Reaction notes

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