Benzeneacetamide, α-hydroxy-N,N-dimethyl-

Benzeneacetamide, α-hydroxy-N,N-dimethyl- Suppliers list
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com
Company Name: Shanxi Xuanran Import and Export Trade Co., Ltd.  
Tel: +8617735180244
Email: mike_yan@xuanranglobal.com
Company Name: Shanghai Kaiwei Chemical Technology Co., Ltd.  
Tel: 021-58461859 15821823057
Email: service@aiviche.com
Company Name: Shanghai Haohong Pharmaceutical Co., Ltd.  
Tel: 400-8210725 4008210725
Email: malulu@leyan.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: marketing1@energy-chemical.com
Benzeneacetamide, α-hydroxy-N,N-dimethyl- Basic information
Product Name:Benzeneacetamide, α-hydroxy-N,N-dimethyl-
Synonyms:Benzeneacetamide, α-hydroxy-N,N-dimethyl-;2-Hydroxy-N,N-dimethyl-2-phenylacetamide
CAS:2019-71-8
MF:C10H13NO2
MW:179.22
EINECS:
Product Categories:
Mol File:2019-71-8.mol
Benzeneacetamide, α-hydroxy-N,N-dimethyl- Structure
Benzeneacetamide, α-hydroxy-N,N-dimethyl- Chemical Properties
Melting point 152-153 °C(Solv: hexane (110-54-3))
Boiling point 321.6±35.0 °C(Predicted)
density 1.135±0.06 g/cm3(Predicted)
storage temp. Store at room temperature
pka12.46±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
Benzeneacetamide, α-hydroxy-N,N-dimethyl- Usage And Synthesis
Synthesis
Benzaldehyde

100-52-7

Silanecarboxamide, pentamethyl- (9CI)

479486-96-9

Benzeneacetamide, α-hydroxy-N,N-dimethyl-

2019-71-8

General procedure: In a Schlenk tube fitted with a PTFE vacuum stopper and a micro-stirring bar, a vacuum flame heating process was carried out followed by argon replacement of the tube atmosphere. Benzaldehyde (1 mmol) and tetrahydrofuran (1 mL) were added to the reaction tube, followed by the addition of N,N-dimethylcarbamoyl (trimethyl) silane (1.2 mmol). After sealing the reaction tube, the mixture was stirred continuously at 60°C until complete consumption of the carbamoylsilane was confirmed by thin layer chromatography (TLC) detection. Upon completion of the reaction, the volatiles were removed under vacuum. The product, 2-hydroxy-N,N-dimethyl-2-phenylacetamide, can be purified by one of the following methods: Kugelrohr distillation, recrystallization from anhydrous ethanol, or separation by column chromatography using a 30-50% light petroleum ether-ethyl acetate solvent mixture as eluent.

References[1] Mendeleev Communications, 2014, vol. 24, # 3, p. 176 - 177
Benzeneacetamide, α-hydroxy-N,N-dimethyl- Preparation Products And Raw materials
Raw materialsBenzaldehyde-->Silanecarboxamide, pentamethyl- (9CI)
Tag:Benzeneacetamide, α-hydroxy-N,N-dimethyl-(2019-71-8) Related Product Information
Benzeneacetamide, α-hydroxy-N-methyl- Mandelic acid diethylamide Benzeneacetamide, α-hydroxy-N,N-dimethyl-, (R)- (9CI) N,N-diMethyl-2-oxo-2-phenylacetaMide 2-Hydroxy-N,N-dimethyl-2-(p-tolyl)acetamide (S)-2-hydroxy-N-Methyl-2-phenylacetaMide