(3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone

Base Information

Chemical Name:(3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone
CAS No.:124716-62-7
Molecular Formula:C₁₆H₂₂N₂O₄
Molecular Weight:306.362
Hs Code.:

Synonyms:(3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone

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Chemical Property of (3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone

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Technology Process of (3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone

There total 4 articles about (3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone 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: 66.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 124816-70-2
(3R)-trans-1-benzyl-3-amino-4-methoxy-β-azetidinone

: 124716-62-7
(3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone

Guidance literature:: With triethylamine; In tert-butyl alcohol; for 6h;
DOI:10.1021/ja00159a034

Reference yield:

: 106501-94-4
methyl N-benzylformimidate

: 124716-62-7
(3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) Na₂Cr(CO)5, Me₃SiCl / 2.) Et₂O, 60 psi, 24 h, irrad.

2: 100 percent / aq. 0.2 N HCl / methanol / 3 h / Ambient temperature

3: 71 percent / H₂ / 20percent Pd(OH)2/C / methanol / 12 h / 735.5 Torr

4: 66 percent / Et₃N / 2-methyl-propan-2-ol / 6 h

With hydrogenchloride; chloro-trimethyl-silane; disodium pentacarbonylchromium; hydrogen; triethylamine; palladium dihydroxide; In methanol; tert-butyl alcohol;
DOI:10.1021/ja00159a034

Reference yield:

: 124716-56-9
(3R,4R)-1-Benzyl-3-((R)-2-hydroxy-1-phenyl-ethylamino)-4-methoxy-azetidin-2-one

: 124716-62-7
(3R)-trans-1-benzyl-3-<<(tert-butyloxy)carbonyl>amino>-4-methoxy-β-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / H₂ / 20percent Pd(OH)2/C / methanol / 12 h / 735.5 Torr

2: 66 percent / Et₃N / 2-methyl-propan-2-ol / 6 h

With hydrogen; triethylamine; palladium dihydroxide; In methanol; tert-butyl alcohol;
DOI:10.1021/ja00159a034