Potassium thioacetate

Potassium thioacetate is an organosulfur compound and a salt with the formula CH3COSK+. This white, water-soluble solid is used as a reagent for preparing thioacetate esters and other derivatives.[1]

Potassium thioacetate
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 233-848-7
MeSH C005732
Properties
C2H3KOS
Molar mass 114.21
Appearance white solid
good
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Synthesis and reactions

Potassium thioacetate, which is commercially available, can be prepared by combining acetyl chloride and potassium hydrogen sulfide: CH3COCl + 2 KSH → KCl + CH3COSK + H2S It arises also by the neutralization of thioacetic acid with potassium hydroxide.

Use in preparation of thiols

In a common application, potassium thioacetate is combined with alkylating agents to give thioacetate esters: CH3COSK + RX → CH3COSR + KX (X = halide) Hydrolysis of these esters affords thiols: CH3COSR + H2O → CH3CO2H + RSH

The thioacetate esters can also be cleaved with methanethiol in the presence of stoichiometric base, as illustrated in the preparation of pent-4-yne-1-thiol:[2]

HC2(CH2)3OMs + KSAc → HC2(CH2)3SAc + KOMs
HC2(CH2)3SAc + HSMe → HC2(CH2)3SH + MeSAc
gollark: It's not great compared to PC, since the vendor can just not provide updates for the vendor stuff, and the kernel is annoying, but you can update much of userspace independently.
gollark: There's a UBPorts GSI.
gollark: Oh, a decent amount, they can use the APIs.
gollark: VoLTE does *not*, and neither does FM radio for some reason, but basically everything else works fine on sane devices.
gollark: With Treble, your phone vendor provides a vendor image on one partition containing something or other, and that provides a bunch of APIs to Android, and thus you can flash a generic system image onto any supported device and basically everything works.

References

  1. Zongjun Qiao and Xuefeng Jiang "Potassium Thioacetate" e-EROS Encyclopedia Of Reagents For Organic Synthesis, 2014. doi:10.1002/047084289X.rn01737
  2. Matteo Minozzi, Daniele Nanni, Piero Spagnolo (2008). "4-Pentyne-1-thiol". eEROS. doi:10.1002/047084289X.rn00855.CS1 maint: uses authors parameter (link)
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.