((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester

Base Information

Chemical Name:((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester
CAS No.:1004791-10-9
Molecular Formula:C₂₂H₃₅NO₆
Molecular Weight:409.523
Hs Code.:

Synonyms:((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester

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Chemical Property of ((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester

Chemical Property:

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Technology Process of ((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester

There total 1 articles about ((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-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:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 79069-63-9,133565-43-2
tert-butyl [(2R,3R)-3-(benzyloxy)-1-hydroxybutan-2-yl]carbamate

: 1004791-10-9
((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester

Guidance literature:: With sodium hydroxide; In water; toluene; at 0 ℃; for 3h;

Reference yield:

: 1004791-10-9
((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester

: 1004791-09-6
(R)-5-((R)-1-benzyloxyethyl)morpholine-3-one

Guidance literature:: ((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;

With thionyl chloride; In methanol; at 20 ℃; for 1h;

With sodium methylate; In methanol; at 0 ℃;

Reference yield:

: 1004791-10-9
((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid t-butyl ester

: 1004791-24-5
(R)-1-[(3R,5R)-5-(4-chlorophenyl)-morpholine-3-yl]ethanol

Guidance literature:: Multi-step reaction with 7 steps

1.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

1.2: 1 h / 20 °C

1.3: 0 °C

2.1: triethylamine / dmap / acetonitrile / 4 h / 20 °C

2.2: 0.5 h / 20 °C

3.1: sodium hydroxide; water / methanol / 3 h / 20 °C

3.2: pH 4

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 20 °C

5.1: tetrahydrofuran / 1 h / -40 - 0 °C

6.1: hydrogenchloride / ethyl acetate / 1 h / 20 °C

6.2: 0 - 20 °C

7.1: trimethylsilyl iodide / dichloromethane / 140 h / 20 °C

With hydrogenchloride; sodium hydroxide; trimethylsilyl iodide; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; dmap; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;