65573-06-0
3-tert-butyl 1-ethyl thiodicarbonate
CAS: 65573-06-0
Molecular Formula: C8H14O3S2
65573-06-0 - Names and Identifiers
65573-06-0 - Physico-chemical Properties
| Molecular Formula | C8H14O3S2 |
| Molar Mass | 222.32 |
65573-06-0 - Introduction
3-tert-butyl 1-ethyl thiodicarbonate is an organic sulfur compound. Its structural formula is:
CH3CH2OC(S)O(C(CH3)3)
The compound has the following properties:
-Appearance is colorless liquid
-The molecular weight is relatively large, about 166.29g/mol
-Strong smell of thiols
-Volatile at room temperature
3-tert-butyl 1-ethyl thiodicarbonate is mainly used for vulcanization reaction in organic synthesis. It can be used as a reagent for alkylation and esterification reactions with thiols (RSH) as substrates. The compounds can also be used as protecting groups, for example alcohols can be protected as thioethers in the synthesis.
The method for preparing 3-tert-butyl 1-ethyl thiodicarbonate is generally by adding 1-ethanol using hydrogen fluoride and Tri (tert-butyl) sulfate chloride to dimethyl sulfoxide, and reacting to generate the target product.
Pay attention to the following safety information when using and storing 3-tert-butyl 1-ethyl thiodicarbonate:
-It should be operated in a well-ventilated place to avoid inhalation of odors
-Avoid contact with skin and eyes to avoid irritation and damage
-Wear appropriate personal protective equipment such as gloves, goggles and lab coats
-Avoid high temperature and fire sources during storage to prevent fire and explosion
-Waste should be disposed of in accordance with local environmental regulations
CH3CH2OC(S)O(C(CH3)3)
The compound has the following properties:
-Appearance is colorless liquid
-The molecular weight is relatively large, about 166.29g/mol
-Strong smell of thiols
-Volatile at room temperature
3-tert-butyl 1-ethyl thiodicarbonate is mainly used for vulcanization reaction in organic synthesis. It can be used as a reagent for alkylation and esterification reactions with thiols (RSH) as substrates. The compounds can also be used as protecting groups, for example alcohols can be protected as thioethers in the synthesis.
The method for preparing 3-tert-butyl 1-ethyl thiodicarbonate is generally by adding 1-ethanol using hydrogen fluoride and Tri (tert-butyl) sulfate chloride to dimethyl sulfoxide, and reacting to generate the target product.
Pay attention to the following safety information when using and storing 3-tert-butyl 1-ethyl thiodicarbonate:
-It should be operated in a well-ventilated place to avoid inhalation of odors
-Avoid contact with skin and eyes to avoid irritation and damage
-Wear appropriate personal protective equipment such as gloves, goggles and lab coats
-Avoid high temperature and fire sources during storage to prevent fire and explosion
-Waste should be disposed of in accordance with local environmental regulations
Last Update：2024-04-09 01:59:54
