(2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

Base Information

Chemical Name:(2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine
CAS No.:1236068-31-7
Molecular Formula:C₁₈H₂₆N₂O₃
Molecular Weight:318.416
Hs Code.:

Synonyms:(2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

Suppliers and Price of (2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

Chemical Property:

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Technology Process of (2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

There total 4 articles about (2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine 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:

Reference yield:

: 104196-23-8
(2S,3S)-2,3-epoxy-3-phenyl-1-propanol

: 1236068-31-7
(2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

Guidance literature:: Multi-step reaction with 4 steps

1.1: dmap; triethylamine / dichloromethane / 0 °C

2.1: pyridine / 20 °C

3.1: sodium azide; ammonium chloride / methanol / 24 h / Reflux

3.2: 10 h / 20 °C / Reflux

4.1: dmap / dichloromethane / 24 h / 20 °C

With pyridine; dmap; sodium azide; ammonium chloride; triethylamine; In methanol; dichloromethane;
DOI:10.1055/s-0030-1260225

Reference yield:

: 104-54-1
3-Phenylpropenol

: 1236068-31-7
(2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

Guidance literature:: Multi-step reaction with 5 steps

1.1: titanium(IV) tetrabutoxide; tert.-butylhydroperoxide / dichloromethane / -20 °C

2.1: dmap; triethylamine / dichloromethane / 0 °C

3.1: pyridine / 20 °C

4.1: sodium azide; ammonium chloride / methanol / 24 h / Reflux

4.2: 10 h / 20 °C / Reflux

5.1: dmap / dichloromethane / 24 h / 20 °C

With pyridine; titanium(IV) tetrabutoxide; tert.-butylhydroperoxide; dmap; sodium azide; ammonium chloride; triethylamine; In methanol; dichloromethane; 1.1: Sharpless asymmetric epoxidation;
DOI:10.1055/s-0030-1260225

Reference yield:

: 1353580-54-7
(2'S,3'S)-4-(3'-phenyloxiran-2'-ylmethyl)morpholine

: 1236068-31-7
(2R,3R)-4-(1-tert-butoxycarbonyl-3-phenylaziridine-2-ylmethyl)morpholine

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium azide; ammonium chloride / methanol / 24 h / Reflux

1.2: 10 h / 20 °C / Reflux

2.1: dmap / dichloromethane / 24 h / 20 °C

With dmap; sodium azide; ammonium chloride; In methanol; dichloromethane;
DOI:10.1055/s-0030-1260225