Sodium borohydride → HCID 57319589, compound

HRID 1895809Notes

Reaction equation

HRID 1895809 reaction equation
[CH:1]([C:3]1[S:7][C:6]([CH:8]=[O:9])=[CH:5][CH:4]=1)=[CH2:2].[BH4-].[Na+]>CO>[CH:1]([C:3]1[S:7][C:6]([CH2:8][OH:9])=[CH:5][CH:4]=1)=[CH2:2]

Participants

4

Conditions

Temperature
0 °C

Procedure

A solution of 5-vinyl-thiophene-2-carbaldehyde (900 mg, 6.4 mmol) in anhydrous methanol (20 mL) was cooled to 0° C. under an atmosphere of nitrogen and treated with sodium borohydride (268 mg, 7.1 mmol). The reaction was stirred at 0° C. for 5 minutes and then at room temperature for 5 minutes, before being quenched with water and concentrated in vacuo. The aqueous layer was extracted twice with dichloromethane, the combined organics dried through a hydrophobic frit and concentrated in vacuo. The product was purified by silica gel chromatography using iso-hexanes/ethyl acetate 7:1 then 2:1 to afford the title compound (800 mg, 88%) as a colourless oil. 1H NMR (300 MHz, CDCl3) δ1.76 (t, J=6.0 Hz, 1H), 4.80 (d, J=6.3 Hz, 2H), 5.15 (d, J=10.7 Hz, 1H), 5.55 (d, J=17.4 Hz, 1H), 6.78 (dd, J=17.4, 10.7 Hz, 1H), 6.85 (d, J=3.6 Hz, 1H), 6.88 (d, J=3.6 Hz, 1H).

Workup

  1. waitat room temperature for 5 minutes
  2. custombefore being quenched with water
  3. concentrationconcentrated in vacuo
  4. extractionThe aqueous layer was extracted twice with dichloromethane
  5. customthe combined organics dried through a hydrophobic frit
  6. concentrationconcentrated in vacuo
  7. customThe product was purified by silica gel chromatography

Sources & evidence

ORD record
ord-018744c726ef49e8bda651ac22444d9c
Source dataset
uspto-grants-2013_08
Patent number
US08513184B2

Reaction notes

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