(R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester

Base Information

Chemical Name:(R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester
CAS No.:331956-17-3
Molecular Formula:C₃₄H₄₅NO₂
Molecular Weight:499.737
Hs Code.:

Synonyms:(R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester

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Chemical Property of (R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester

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Technology Process of (R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester

There total 4 articles about (R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl 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: 98.0%

: 52745-93-4
(4R)-4-methylhexanoic acid

: 331956-09-3
(1R,2S)-2-[(2-methylbenzyl)(2,4,6-trimethylbenzylamino)]-1-phenylpropan-1-ol

: 331956-17-3
(R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 6h;
DOI:10.1021/jo001293h

Reference yield:

: 487-68-3
mesytaldehyde

: 331956-17-3
(R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: MgSO₄ / toluene / 6 h / 80 °C

1.2: 65 percent / AcOH; NaCNBH₃ / methanol / 3 h / 20 °C

2.1: 95 percent / toluene; acetonitrile / 1 h / 90 °C

3.1: 98 percent / EDCI*HCl; DMAP / CH₂Cl₂ / 6 h / 20 °C

With dmap; magnesium sulfate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; toluene; acetonitrile;
DOI:10.1021/jo001293h

Reference yield:

: 492-41-1,58550-13-3,757124-50-8
(1R,2S)-norephedrine

: 331956-17-3
(R)-4-Methyl-hexanoic acid (1R,2S)-2-[(2-methyl-benzyl)-(2,4,6-trimethyl-benzyl)-amino]-1-phenyl-propyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: MgSO₄ / toluene / 6 h / 80 °C

1.2: 65 percent / AcOH; NaCNBH₃ / methanol / 3 h / 20 °C

2.1: 95 percent / toluene; acetonitrile / 1 h / 90 °C

3.1: 98 percent / EDCI*HCl; DMAP / CH₂Cl₂ / 6 h / 20 °C

With dmap; magnesium sulfate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; toluene; acetonitrile;
DOI:10.1021/jo001293h