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2-{(3R)-4-[1-(diphenylmethyl)azetidin-3-yl]morpholin-3-yl}ethanol

Base Information Edit
  • Chemical Name:2-{(3R)-4-[1-(diphenylmethyl)azetidin-3-yl]morpholin-3-yl}ethanol
  • CAS No.:917572-33-9
  • Molecular Formula:C22H28N2O2
  • Molecular Weight:352.477
  • Hs Code.:
  • Mol file:917572-33-9.mol
2-{(3R)-4-[1-(diphenylmethyl)azetidin-3-yl]morpholin-3-yl}ethanol

Synonyms:2-{(3R)-4-[1-(diphenylmethyl)azetidin-3-yl]morpholin-3-yl}ethanol

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Chemical Property of 2-{(3R)-4-[1-(diphenylmethyl)azetidin-3-yl]morpholin-3-yl}ethanol Edit
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Technology Process of 2-{(3R)-4-[1-(diphenylmethyl)azetidin-3-yl]morpholin-3-yl}ethanol

There total 6 articles about 2-{(3R)-4-[1-(diphenylmethyl)azetidin-3-yl]morpholin-3-yl}ethanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
N-benzhydryl 3-azetidinone; 2-[(3R)-morpholin-3-yl]ethanol; With (polystyrylmethyl)trimethylammonium cyanoborohydride; acetic acid; In methanol; at 120 ℃; for 0.0833333h; Polystyrene Microwave irradiation;
With water; sodium hydrogencarbonate;
Guidance literature:
Multi-step reaction with 5 steps
1: sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate / dichloromethane; water / 20 h / Heating / reflux
2: hydrogenchloride / 20 °C
3: lithium aluminium tetrahydride / diethyl ether / 1 h / 20 °C
4: hydrogen; acetic acid / palladium(II) hydroxide/carbon / 17 h / 20 °C / 3000.3 Torr
5: (polystyrylmethyl)trimethylammonium cyanoborohydride; acetic acid / methanol / 0.08 h / 120 °C / Microwave irradiation
With hydrogenchloride; sodium hydroxide; lithium aluminium tetrahydride; (polystyrylmethyl)trimethylammonium cyanoborohydride; hydrogen; tetra(n-butyl)ammonium hydrogensulfate; acetic acid; palladium(II) hydroxide/carbon; In methanol; diethyl ether; dichloromethane; water;
Guidance literature:
Multi-step reaction with 4 steps
1: hydrogenchloride / 20 °C
2: lithium aluminium tetrahydride / diethyl ether / 1 h / 20 °C
3: hydrogen; acetic acid / palladium(II) hydroxide/carbon / 17 h / 20 °C / 3000.3 Torr
4: (polystyrylmethyl)trimethylammonium cyanoborohydride; acetic acid / methanol / 0.08 h / 120 °C / Microwave irradiation
With hydrogenchloride; lithium aluminium tetrahydride; (polystyrylmethyl)trimethylammonium cyanoborohydride; hydrogen; acetic acid; palladium(II) hydroxide/carbon; In methanol; diethyl ether;
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