Sodium borohydride → HCID 86722584, compound

HRID 1502788Notes

Reaction equation

HRID 1502788 reaction equation
[BH4-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([CH:11]=[C:12]([Br:15])[C:13]=1[Cl:14])[C:7](OC)=[O:8]>CO>[Br:3][C:4]1[CH:5]=[C:6]([CH2:7][OH:8])[CH:11]=[C:12]([Br:15])[C:13]=1[Cl:14]

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 86722585HCID 86722585, compound

Product 1

HCID 86722584HCID 86722584, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

NaBH4 (1.53 g, 40.65 mmol) was added portionwise to a stirred solution of methyl 3,5-dibromo-4-chlorobenzoate (4.45 g, 13.6 mmol) in MeOH (50 mL) at 0° C. The reaction mixture was then stirred at ambient temperature for 8 h. The volatiles were evaporated and the residue was diluted with CH2Cl2 and washed with brine followed by water. The organic layer was dried (Na2SO4), filtered and concentrated to afford the title compound as an off white solid (3.3 g, 80%): 1H NMR (300 MHz, DMSO-d6) δ 7.71 (s, 2H), 5.49 (bs, 1H), 4.48 (d, J=4.5 Hz, 2H); ESIMS m/z 297.9 ([M]+); IR (thin film) 3460, 747, 534 cm−1.

Workup

  1. customThe volatiles were evaporated
  2. additionthe residue was diluted with CH2Cl2
  3. washwashed with brine
  4. dry with materialThe organic layer was dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-ee71d106e9a14ef2a03535d314f41e9a
Source dataset
uspto-grants-2015_12
Patent number
US09210927B2

Reaction notes

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