(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Base Information

Chemical Name:(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone
CAS No.:195607-04-6
Molecular Formula:C₁₉H₂₀N₂O₆
Molecular Weight:372.378
Hs Code.:

Synonyms:(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

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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 (4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

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Technology Process of (4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

There total 4 articles about (4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone 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: 78.0%

: 195607-03-5
(S)-1-(4-Benzyloxy-5-methoxy-2-nitro-benzoyl)-azetidine-2-carboxylic acid methyl ester

: 195607-04-6
(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Guidance literature:: With lithium borohydride; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1016/S0040-4039(97)01297-5

Reference yield:

: 64154-78-5
4-benzyloxy-5-methoxy-2-nitrobenzoyl chloride

: 195607-04-6
(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N

2: SOCl₂

3: 78 percent / lithium borohydride / tetrahydrofuran / 0 - 20 °C

With lithium borohydride; thionyl chloride; triethylamine; In tetrahydrofuran;
DOI:10.1016/S0040-4039(97)01297-5

Reference yield:

: 60547-92-4
4-(benzyloxy)-5-methoxy-2-nitrobenzoic acid

: 195607-04-6
(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-((S)-2-hydroxymethyl-azetidin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl chloride / tetrahydrofuran

2: Et₃N

3: SOCl₂

4: 78 percent / lithium borohydride / tetrahydrofuran / 0 - 20 °C

With lithium borohydride; thionyl chloride; oxalyl dichloride; triethylamine; In tetrahydrofuran;
DOI:10.1016/S0040-4039(97)01297-5