4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid

Base Information

• Chemical Name: 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid
• CAS No.: 844873-54-7
• Molecular Formula: C₂₁H₃₁NO₆
• Molecular Weight: 393.48
• Mol file: 844873-54-7.mol

Synonyms:4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid

Chemical Property of 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid

There total 5 articles about 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid 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: 85.0%

tert-Butyl (+/-)-4-(3-cyclopentyloxy-4-methoxyphenyl)-pyrrolidin-2-one-1-carboxylate (360042-78-0) → 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid (844873-54-7)

Guidance literature:

With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 2h;

DOI:10.1021/jo0484880

Reference yield:

N-(tert-butoxycarbonyl)-3-pyrroline (73286-70-1) → 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid (844873-54-7)

Guidance literature:

Multi-step reaction with 3 steps

1: Pd(OAc)2; H₂O / acetonitrile / 0.75 h / 30 °C

2: tetrapropylammonium perruthenate; N-methylmorpholine N-oxide / CH₂Cl₂ / 3 h / 20 °C

3: 85 percent / LiOH / tetrahydrofuran; H₂O / 2 h / 20 °C

With palladium diacetate; lithium hydroxide; tetrapropylammonium perruthennate; water; 4-methylmorpholine N-oxide; In tetrahydrofuran; dichloromethane; water; acetonitrile; 1: Heck-Matsuda arylation;

DOI:10.1021/jo0484880

Reference yield:

1-(tert-butoxycarbonyl)-4-(3-cyclopentyloxy-4-methoxyphenyl)pyrrolidin-2-ol (844873-53-6) → 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid (844873-54-7)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrapropylammonium perruthenate; N-methylmorpholine N-oxide / CH₂Cl₂ / 3 h / 20 °C

2: 85 percent / LiOH / tetrahydrofuran; H₂O / 2 h / 20 °C

With lithium hydroxide; tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide; In tetrahydrofuran; dichloromethane; water;

DOI:10.1021/jo0484880

upstream raw materials:

tert-Butyl (+/-)-4-(3-cyclopentyloxy-4-methoxyphenyl)-pyrrolidin-2-one-1-carboxylate

N-(tert-butoxycarbonyl)-3-pyrroline

1-(tert-butoxycarbonyl)-4-(3-cyclopentyloxy-4-methoxyphenyl)pyrrolidin-2-ol