(3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

Base Information

Chemical Name:(3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone
CAS No.:1342305-98-9
Molecular Formula:C₂₁H₂₃NO₅
Molecular Weight:369.417
Hs Code.:

Synonyms:(3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

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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 (3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

Chemical Property:

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Technology Process of (3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

There total 5 articles about (3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-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: 98.0%

: 1342305-96-7
(3S,4S)-4-p-benzyloxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

: 1342305-98-9
(3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 4h; under 1551.49 Torr;
DOI:10.1016/j.ejmech.2011.08.025

Reference yield:

: 1342305-93-4
C₂₅H₂₇NO₄

: 1342305-98-9
(3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

Guidance literature:: Multi-step reaction with 3 steps

1: trichloroacetonitrile; triphenylphosphine / tetrahydrofuran / 1 h / 0 - 20 °C

2: tert-butylimino-tri(pyrrolidino)phosphorane / acetonitrile / 20 °C

3: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 1551.49 Torr

With palladium 10% on activated carbon; hydrogen; trichloroacetonitrile; triphenylphosphine; tert-butylimino-tri(pyrrolidino)phosphorane; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1016/j.ejmech.2011.08.025

Reference yield:

: 1342305-94-5
C₂₈H₃₀ClNO₅

: 1342305-98-9
(3S,4S)-4-p-hydroxybenzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: tert-butylimino-tri(pyrrolidino)phosphorane / acetonitrile / 20 °C

2: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 1551.49 Torr

With palladium 10% on activated carbon; hydrogen; tert-butylimino-tri(pyrrolidino)phosphorane; In methanol; acetonitrile;
DOI:10.1016/j.ejmech.2011.08.025