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

Base Information

Chemical Name:tert-butoxycarbonylamino-acetic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester
CAS No.:264888-35-9
Molecular Formula:C₂₇H₃₇NO₆
Molecular Weight:471.594
Hs Code.:

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

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

Suppliers and Price of tert-butoxycarbonylamino-acetic acid 3-(3-benzyloxy-6-hydroxy-2,4-dimethyl-phenyl)-3-methyl-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

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

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

There total 4 articles about tert-butoxycarbonylamino-acetic 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: 99.0%

: 4530-20-5
BOC-glycine

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

: 264888-35-9
tert-butoxycarbonylamino-acetic 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

: 264888-35-9
tert-butoxycarbonylamino-acetic 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: 99 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

: 264888-35-9
tert-butoxycarbonylamino-acetic 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: 99 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