Sodium borohydride → HCID 10198426, compound

HRID 1954929Notes

Reaction equation

HRID 1954929 reaction equation
[F:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[C:4](=[O:16])[CH2:5]/[C:6]/2=[CH:12]\[C:13]([NH2:15])=[O:14].[BH4-].[Na+]>C(O)C>[F:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH:4]([OH:16])[CH2:5]/[C:6]/2=[CH:12]\[C:13]([NH2:15])=[O:14]

Participants

4

Procedure

A suspension of (E)-2-(4,6-difluoro-3-oxo-1-indanylidene)acetamide (0.100 g, 0.45 mmol) and sodium borohydride (0.017 g, 0.45 mmol) in 95% ethanol was stirred at ambient temperature for 2 hours. The mixture was cooled in an ice bath and quenched with 0.1N hydrochloric acid (3 mL). The ethanol was evaporated in vacuo, and the residue was dissolved in ethyl acetate (50 mL), washed successively with water (2×30 mL) and brine (30 mL), dried over sodium sulfate, filtered, and evaporated in vacuo. The resudue was washed successively with cold ethyl acetate, hexane, and diethyl ether to give 0.046 g (45%) of (E)-2-(4,6-difluoro-3-hydroxy-1-indanylidene)acetamide as a white solid; mp 232-237° C. (dec.) 1H-NMR (DMSO-d6): δ7.06-7.42 (m, 4H), 6.49 (s, 1H), 5.52 (d, 1H), 5.30 (m, 1H), 3.44 (m, 1H), 3.03 (d, 1H).

Workup

  1. temperatureThe mixture was cooled in an ice bath
  2. customquenched with 0.1N hydrochloric acid (3 mL)
  3. customThe ethanol was evaporated in vacuo
  4. dissolutionthe residue was dissolved in ethyl acetate (50 mL)
  5. washwashed successively with water (2×30 mL) and brine (30 mL)
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated in vacuo
  9. washThe resudue was washed successively with cold ethyl acetate, hexane, and diethyl ether

Sources & evidence

ORD record
ord-a5155c48a1514b318cbcfe324ad990a3
Source dataset
uspto-grants-2000_09
Patent number
US06124284

Reaction notes

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