911300-60-2

Basic information

• Product Name: tert-butyl (3-methoxypropyl)carbamate
• Synonyms: tert-butyl (3-methoxypropyl)carbamate
• CAS NO: 911300-60-2
• Molecular Weight: 189.255
• Mol File: 911300-60-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl (3-methoxypropyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (3-methoxypropyl)carbamate(911300-60-2)
• EPA Substance Registry System: tert-butyl (3-methoxypropyl)carbamate(911300-60-2)

Safety Data

• Hazardous Substances Data: 911300-60-2(Hazardous Substances Data)

Upstream product

• 58885-58-8 N-tert-butoxycarbonyl-3-aminopropanol 
• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 

Downstream Products

• 1610605-40-7 tert-butyl ethyl(3-methoxy-1-phenylpropyl)carbamate 
• 18600-41-4 3-methoxypropan-1-amine hydrochloride 

Relevant articles and documents

Method for preparing amino ether compounds

The invention belongs to the technical field of organic synthesis and relates to a method for preparing amino ether compounds. The method comprises the following steps: by taking amino alcohol as a raw material, protecting amino in the amino alcohol so as to obtain Schiff base; carrying out an etherification reaction on the hydroxyl group in the Schiff base; and finally, performing amino deprotection, thereby obtaining corresponding amino ethers. The method disclosed by the invention has high regio-selectivity, the substrates of higher than 99.9% are subjected to etherification reaction, the reaction conversion ratio of each step is higher than 99.8%, and the total yield is higher than 95%; when amino alcohol is chiral, the amino ethers with retention of configuration can be obtained; and moreover, each step of the method is a conventional operation, the process cost is low, and three wastes are few, the energy consumption is low, an environment-friendly effect is achieved, and large-scale industrial production is easily realized.