ChemicalBook--->CAS DataBase List--->40023-74-3

40023-74-3

40023-74-3 Structure

40023-74-3 Structure
IdentificationBack Directory
[Name]

1-(2-METHOXY-PHENYL)-ETHYLAMINE
[CAS]

40023-74-3
[Synonyms]

AURORA KA-7736
ASINEX-REAG BAS 05269105
1-(2-METHOXYPHENYL)ETHANAMINE
2-Methoxy-α-methylbenzylamine
1-(2-METHOXY-PHENYL)-ETHYLAMINE
2-Methoxy-α-methylbenzenemethanamine
Benzenemethanamine, 2-methoxy-a-methyl-
Benzenemethanamine, 2-methoxy-α-methyl-
BenzeneMethanaMine, 2-Methoxy-.alpha.-Methyl-
[Molecular Formula]

C9H13NO
[MDL Number]

MFCD00593475
[MOL File]

40023-74-3.mol
[Molecular Weight]

151.21
Chemical PropertiesBack Directory
[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
[pka]

9.13±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314-H318
[Precautionary statements ]

P260-P264-P280-P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P305+P351+P338-P405-P501-P280-P305+P351+P338-P310
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[RIDADR ]

UN2735
[HazardClass ]

IRRITANT
[HS Code ]

2922290090
Spectrum DetailBack Directory
[Spectrum Detail]

1-(2-METHOXY-PHENYL)-ETHYLAMINE(40023-74-3)1HNMR
Hazard InformationBack Directory
[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
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