Réaction #155412

ord-80938e306ddf4358b1a02ccf299ce800

Équation de réaction

[Al+3].[H-].[H-].[H-].[H-].[Li+]
Lithium aluminium hydride
N#CSc1ccc(O)c(Cl)c1
3-chloro-4-hydroxyphenyl thiocyanate
Oc1ccc(S)cc1Cl
2-chloro-4-mercaptophenol
Rendement 100.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe mixture was cooled to 5° C.
  2. 2
    Autrequenched with a 1:1 mixture of tetrahydrofuran
  3. 3
    workup.ADDITION1N hydrochloric acid solution in water (30 mL) was then added
  4. 4
    Extractionthe mixture extracted with ethyl acetate (2-fold 70 mL)
  5. 5
    SéchageThe combined organic layers were dried (sodium sulphate)
  6. 6
    Concentrationconcentrated in vacuo
  7. 7
    Autreaffording a colourless crystalline solid, 100% yield, 3.60 g

Mode opératoire

Lithium aluminium hydride (as a 1M solution in tetrahydrofuran, 71.0 ml, 71.0 mmol) was added dropwise to an ice cold solution of 3-chloro-4-hydroxyphenyl thiocyanate (4.20 g, 22.6 mmol) in tetrahydrofuran (100 mL) under nitrogen. The reaction mixture was stirred and allowed to warm to room temperature over 5 hours. The mixture was cooled to 5° C. and quenched with a 1:1 mixture of tetrahydrofuran:water until no more gas evolution was seen. 1N hydrochloric acid solution in water (30 mL) was then added, and the mixture extracted with ethyl acetate (2-fold 70 mL). The combined organic layers were dried (sodium sulphate) and concentrated in vacuo affording a colourless crystalline solid, 100% yield, 3.60 g.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08822439B2uspto-grants-2014_09