69373-87-1

Basic information

• Product Name: ethyl 2-(3,4-diethoxyphenyl)acetate
• Synonyms: ethyl 2-(3,4-diethoxyphenyl)acetate
• CAS NO: 69373-87-1
• Molecular Weight: 252.31
• Mol File: 69373-87-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl 2-(3,4-diethoxyphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(3,4-diethoxyphenyl)acetate(69373-87-1)
• EPA Substance Registry System: ethyl 2-(3,4-diethoxyphenyl)acetate(69373-87-1)

Safety Data

• Hazardous Substances Data: 69373-87-1(Hazardous Substances Data)

Upstream product

• 7664-93-9 sulfuric acid 
• 53017-34-8 ethyl 2-(3,4-diethoxyphenyl)-2-oxoacetate 
• 10035-10-6 hydrogen bromide 
• 64-19-7 acetic acid 
• 2050-46-6 1,2-diethoxybenzene 
• 53207-08-2 4-bromo-1,2-diethoxybenzene 
• 17345-77-6 1-bromo-3,4-dihydroxybenzene 
• 1005009-95-9 2-(3,4-diethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 105-36-2 ethyl bromoacetate 

Downstream Products

• 6298-46-0 N-(3,4-diethoxyphenylacetyl)-β-(3,4-diethoxyphenyl)ethylamine 
• 911-60-4 1-(3',4'-diethoxybenzyl)-6,7-diethoxy-3,4-dihydroisoquinoline hydrochloride 
• 526190-09-0 2-(3,4-diethoxyphenyl)acetamide 
• 61381-04-2 2-(3,4-diethoxyphenyl)ethylamine 
• 985-12-6 1-(3,4-diethoxybenzylidene)-6,7-diethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 38464-04-9 3,4-diethoxy-phenyl-acetic acid 

Relevant articles and documents

Novel method for preparing drotaverine hydrochloride intermediate

The invention discloses a novel method for preparing a drotaverine hydrochloride intermediate, belonging to the technical field of medicine synthesis. The preparation method comprises the following steps: preparing an intermediate 3,4-diethoxyphenylacetic acid with 1,2-diethoxybenzene as a raw material, and preparing the intermediate 3,4-diethoxyphenylacetamide with 3,4-diethoxyphenylacetic acid as a raw material. According to the novel process for preparing the drotaverine hydrochloride intermediate, a method for directly preparing 3,4-diethoxyphenylacetic acid and 3,4-diethoxyphenylethylamine is adopted, and a process for preparing 3,4-diethoxyphenylacetonitrile is avoided, so a reaction step of using sodium cyanide is avoided.