(4-CHLORO-3-METHOXYPHENYL)ACETONITRILE
- Product Name
- (4-CHLORO-3-METHOXYPHENYL)ACETONITRILE
- CAS No.
- 13726-21-1
- Chemical Name
- (4-CHLORO-3-METHOXYPHENYL)ACETONITRILE
- Synonyms
- RARECHEM AL MP 0203;2-(4-Chloro-3-methoxyphenyl);(4-CHLORO-3-METHOXYPHENYL)ACETONITRILE;2-(4-Chloro-3-Methoxyphenyl)acetonitrile;Benzeneacetonitrile, 4-chloro-3-methoxy-;2-(4-Chloro-3-methoxyphenyl)acetonitrilev
- CBNumber
- CB82452470
- Molecular Formula
- C9H8ClNO
- Formula Weight
- 181.62
- MOL File
- 13726-21-1.mol
(4-CHLORO-3-METHOXYPHENYL)ACETONITRILE Property
- Melting point:
- 170-178 °C
- Boiling point:
- 297.5±25.0 °C(Predicted)
- Density
- 1.198±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- White to light yellow Solid
N-Bromosuccinimide Price
- Product number
- 6563AA
- Product name
- 2-(4-Chloro-3-methoxyphenyl)acetonitrile
- Packaging
- 1g
- Price
- $447
- Updated
- 2021/12/16
- Product number
- 116087
- Product name
- (4-Chloro-3-methoxyphenyl)acetonitrile
- Purity
- >97%
- Packaging
- 500mg
- Price
- $544
- Updated
- 2021/12/16
- Product number
- 116087
- Product name
- (4-Chloro-3-methoxyphenyl)acetonitrile
- Purity
- >97%
- Packaging
- 1g
- Price
- $730
- Updated
- 2021/12/16
- Product number
- HCH0314348
- Product name
- 4-CHLORO-3-METHOXY-BENZENEACETONITRILE
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $808.5
- Updated
- 2021/12/16
- Product number
- A861924
- Product name
- 2-(4-Chloro-3-methoxyphenyl)acetonitrile
- Purity
- 98%
- Packaging
- 100mg
- Price
- $49
- Updated
- 2021/12/16
(4-CHLORO-3-METHOXYPHENYL)ACETONITRILE Chemical Properties,Usage,Production
Synthesis
143-33-9
103347-14-4
13726-21-1
To a 90% ethanol (500 mL) solution of 4-(bromomethyl)-1-chloro-2-methoxybenzene (68.5 g, 0.290 mol) was added sodium cyanide (28.5 g, 0.580 mol). The reaction mixture was stirred at 60 °C overnight. Upon completion of the reaction, the ethanol was removed by evaporation under reduced pressure and the residue was dissolved in water. The aqueous phase was extracted with ethyl acetate (300 mL × 3). The organic layers were combined, washed with saturated saline, and dried over anhydrous sodium sulfate. Purification by silica gel column chromatography (eluent: petroleum ether/ethyl acetate = 30:1) afforded 4-chloro-3-methoxyphenylacetonitrile (25 g, 48% yield).1H NMR (400 MHz, CDCl3) δ 7.36 (d, J = 8 Hz, 1H), 6.88-6.84 (m, 2H), 3.92 (s, 3H), 3.74 (s, 2H ).13C NMR (100 MHz, CDCl3) δ 155.4, 130.8, 129.7, 122.4, 120.7, 117.5, 111.5, 56.2, 23.5.
References
[1] Patent: US2007/244159, 2007, A1. Location in patent: Page/Page column 91
[2] Patent: US2005/239881, 2005, A1. Location in patent: Page/Page column 27
[3] Patent: WO2007/39736, 2007, A1. Location in patent: Page/Page column 28
[4] Patent: US2008/293775, 2008, A1. Location in patent: Page/Page column 22
[5] Patent: US2004/192704, 2004, A1. Location in patent: Page 23
(4-CHLORO-3-METHOXYPHENYL)ACETONITRILE Preparation Products And Raw materials
Raw materials
Preparation Products
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