1-(2-METHOXY-PHENYL)-ETHYLAMINE

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Products Intro: Product Name:1-(2-METHOXY-PHENYL)-ETHYLAMINE
CAS:40023-74-3
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CAS:40023-74-3
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CAS:40023-74-3
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CAS:40023-74-3
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Products Intro: Product Name:1-(2-Methoxyphenyl)ethanamine
CAS:40023-74-3
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1-(2-METHOXY-PHENYL)-ETHYLAMINE manufacturers

1-(2-METHOXY-PHENYL)-ETHYLAMINE Basic information
Product Name:1-(2-METHOXY-PHENYL)-ETHYLAMINE
Synonyms:AURORA KA-7736;ASINEX-REAG BAS 05269105;1-(2-METHOXYPHENYL)ETHANAMINE;1-(2-METHOXY-PHENYL)-ETHYLAMINE;2-Methoxy-α-methylbenzenemethanamine;2-Methoxy-α-methylbenzylamine;BenzeneMethanaMine, 2-Methoxy-.alpha.-Methyl-;Benzenemethanamine, 2-methoxy-a-methyl-
CAS:40023-74-3
MF:C9H13NO
MW:151.21
EINECS:
Product Categories:
Mol File:Mol File
1-(2-METHOXY-PHENYL)-ETHYLAMINE Structure
1-(2-METHOXY-PHENYL)-ETHYLAMINE Chemical Properties
Boiling point 244.1±23.0 °C(Predicted)
density 1.003±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka9.13±0.10(Predicted)
AppearanceColorless to light yellow Liquid
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
RIDADR UN2735
HazardClass IRRITANT
HS Code 2922290090
MSDS Information
1-(2-METHOXY-PHENYL)-ETHYLAMINE Usage And Synthesis
Synthesis
2'-Methoxyacetophenone

579-74-8

1-(2-METHOXY-PHENYL)-ETHYLAMINE

40023-74-3

GENERAL PROCEDURE: To a saturated NH4OAc ethanol solution (40 mL) was added activated zinc powder (5 eq.), 2'-methoxyacetophenone (1 eq.), NaBH3CN (3 eq.), and 30% aqueous ammonia solution (10 mL), in that order. The reaction mixture was stirred at 80 °C for 36 hours. After completion of the reaction, it was cooled to room temperature and concentrated under reduced pressure. The residue was dissolved with dichloromethane and adjusted to alkaline with 1 M NaOH aqueous solution (50 mL). The organic phase was separated and the aqueous phase was back-extracted with dichloromethane (2 x 25 mL). The organic phases were combined and acidified with HCl to pH 2.0. The organic layer was separated and the aqueous layer was extracted with dichloromethane (2 x 25 mL). After the aqueous layer was adjusted to pH 10.0 with NaOH, the organic layer was extracted with dichloromethane (3 × 25 mL). The organic layers were combined, dried with anhydrous Na2SO4 and the solvent was evaporated under reduced pressure to obtain the target product 1-(2-methoxyphenyl)ethylamine.

References[1] Science, 2017, vol. 358, # 6361, p. 326 - 332
[2] Chemistry - A European Journal, 2014, vol. 20, # 1, p. 245 - 252
[3] Farmaco, 1991, vol. 46, # 7-8, p. 861 - 872
[4] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 13, p. 3592 - 3602
[5] Chirality, 2018, vol. 30, # 7, p. 900 - 906
1-(2-METHOXY-PHENYL)-ETHYLAMINE Preparation Products And Raw materials
Raw materials2'-Methoxyacetophenone-->Ammonium acetate-->ZINC-->Ethanol-->Sodium cyanoborohydride-->Ammonium hydroxide-->Water
Tag:1-(2-METHOXY-PHENYL)-ETHYLAMINE(40023-74-3) Related Product Information

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