2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester

Base Information

• Chemical Name: 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester
• CAS No.: 237394-33-1
• Molecular Formula: C₃₃H₄₄NO₆P
• Molecular Weight: 581.689

Synonyms:2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester

Chemical Property of 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester

Chemical Property:

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Technology Process of 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester

There total 3 articles about 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl 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: 97.0%

1-Adamantyl bromide (768-90-1) + 2-[(1-benzyloxycarbonylamino-ethyl)-hydroxy-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester (237394-19-3) → 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester (237394-33-1)

Guidance literature:

With silver(l) oxide; In chloroform; for 0.5h; Heating;

DOI:10.1021/jm9900164

Reference yield:

ethyl 2-phenethylpropenoate (27356-87-2) → 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester (237394-33-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) hexamethyldisilazane / 1.) 110 deg C, 1 h, 2.) 110 deg C, 3 h

2: 97 percent / silver oxide / CHCl₃ / 0.5 h / Heating

With 1,1,1,3,3,3-hexamethyl-disilazane; silver(l) oxide; In chloroform;

DOI:10.1021/jm9900164

Reference yield:

[1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid (108327-37-3) → 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester (237394-33-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) hexamethyldisilazane / 1.) 110 deg C, 1 h, 2.) 110 deg C, 3 h

2: 97 percent / silver oxide / CHCl₃ / 0.5 h / Heating

With 1,1,1,3,3,3-hexamethyl-disilazane; silver(l) oxide; In chloroform;

DOI:10.1021/jm9900164

upstream raw materials:

1-Adamantyl bromide

2-[(1-benzyloxycarbonylamino-ethyl)-hydroxy-phosphinoylmethyl]-4-phenyl-butyric acid ethyl ester

ethyl 2-phenethylpropenoate

[1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid

Downstream raw materials:

2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-ethyl)-phosphinoylmethyl]-4-phenyl-butyric acid

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