(E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester

Base Information

Chemical Name:(E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester
CAS No.:717127-61-2
Molecular Formula:C₂₅H₃₁NO₆
Molecular Weight:441.524
Hs Code.:

Synonyms:(E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester

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Chemical Property of (E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester

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Technology Process of (E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester

There total 5 articles about (E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester 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: 81.0%

: 89238-99-3
O-(4-methoxybenzyl)-trichloroacetimidate

: 717127-98-5
(E)-2-Benzyloxycarbonylamino-5-hydroxymethyl-hept-4-enoic acid methyl ester

: 717127-61-2
(E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester

Guidance literature:: boron trifluoride diethyl etherate; at 20 ℃; for 3h;
DOI:10.1016/j.tetlet.2004.03.089

Reference yield:

: 65305-57-9
Acetic acid (E)-4-chloro-2-ethyl-but-2-enyl ester

: 717127-61-2
(E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: TBABr; KI; K₂CO₃ / acetonitrile / Heating

2: aq. HCl / 0.5 h

3: 96 percent / K₂CO₃ / CH₂Cl₂

4: 95 percent / K₂CO₃ / methanol

5: 81 percent / BF₃*OEt₂ / 3 h / 20 °C

With hydrogenchloride; tetrabutylammomium bromide; potassium carbonate; potassium iodide; boron trifluoride diethyl etherate; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.tetlet.2004.03.089

Reference yield:

: 717127-53-2
(E)-5-Acetoxymethyl-2-amino-hept-4-enoic acid methyl ester

: 717127-61-2
(E)-2-Benzyloxycarbonylamino-5-(4-methoxy-benzyloxymethyl)-hept-4-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / K₂CO₃ / CH₂Cl₂

2: 95 percent / K₂CO₃ / methanol

3: 81 percent / BF₃*OEt₂ / 3 h / 20 °C

With potassium carbonate; boron trifluoride diethyl etherate; In methanol; dichloromethane;
DOI:10.1016/j.tetlet.2004.03.089