2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

Base Information

Chemical Name:2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester
CAS No.:264888-34-8
Molecular Formula:C₃₁H₄₅NO₆
Molecular Weight:527.701
Hs Code.:

2-<i>tert</i>-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

Synonyms:2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

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Chemical Property of 2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

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Technology Process of 2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

There total 4 articles about 2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl 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: 100.0%

: 13139-15-6,53296-34-7
N-tert-butoxycarbonyl-L-leucine

: 157547-47-2
3-(2'-Hydroxy-5'-benzyloxy-4',6'-dimethylphenyl)-3,3-dimethyl-1-propanol

: 264888-34-8
2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

Guidance literature:: With dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1248/cpb.48.238

Reference yield:

: 50442-68-7
6-hydroxy-4,4,5,7-tetramethyl-3,4-dihydrocoumarin

: 264888-34-8
2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / K₂CO₃; NaI / acetone / 20 h / Heating

2: 97 percent / LiAlH₄ / tetrahydrofuran / 7 h / 20 °C

3: 100 percent / EDC; DMAP / CH₂Cl₂ / 5 h / 20 °C

With dmap; lithium aluminium tetrahydride; potassium carbonate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; sodium iodide; In tetrahydrofuran; dichloromethane; acetone; 1: Alkylation / 2: Reduction / 3: Acylation;
DOI:10.1248/cpb.48.238

Reference yield:

: 100-44-7
benzyl chloride

: 264888-34-8
2-tert-butoxycarbonylamino-4-methyl-pentanoic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / K₂CO₃; NaI / acetone / 20 h / Heating

2: 97 percent / LiAlH₄ / tetrahydrofuran / 7 h / 20 °C

3: 100 percent / EDC; DMAP / CH₂Cl₂ / 5 h / 20 °C

With dmap; lithium aluminium tetrahydride; potassium carbonate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; sodium iodide; In tetrahydrofuran; dichloromethane; acetone; 1: Alkylation / 2: Reduction / 3: Acylation;
DOI:10.1248/cpb.48.238