Réaction #155412
ord-80938e306ddf4358b1a02ccf299ce800
Équation de réaction
Lithium aluminium hydride
3-chloro-4-hydroxyphenyl thiocyanate
→
2-chloro-4-mercaptophenol
Rendement 100.0%
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1TempératureThe mixture was cooled to 5° C.
- 2Autrequenched with a 1:1 mixture of tetrahydrofuran
- 3workup.ADDITION1N hydrochloric acid solution in water (30 mL) was then added
- 4Extractionthe mixture extracted with ethyl acetate (2-fold 70 mL)
- 5SéchageThe combined organic layers were dried (sodium sulphate)
- 6Concentrationconcentrated in vacuo
- 7Autreaffording 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.