[(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester
CAS No.:603127-09-9
Molecular Formula:C₃₇H₆₇NO₉
Molecular Weight:669.94
Hs Code.:

Synonyms:[(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

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Chemical Property of [(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

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Technology Process of [(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

There total 7 articles about [(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-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%

: 107-30-2
chloromethyl methyl ether

: 603127-08-8
[(1S,12S)-1-((1R,2R)-2-Benzyloxy-3-hydroxy-1-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

: 603127-09-9
[(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1016/S0040-4039(02)02743-0

Reference yield:

: (S)-11-Methoxymethoxy-13-methyl-tetradec-1-yne

: 603127-09-9
[(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: BuLi / tetrahydrofuran / -78 - 0 °C

1.2: PCC; 4 A MS / CH₂Cl₂

2.1: CAN / acetonitrile; H₂O

2.2: DMAP; Et₃N / CH₂Cl₂

3.1: 95 percent / HCOOH; methanol / Pd

4.1: 74 percent / Ag₂O / ethyl acetate

5.1: 100 percent / (i-Pr)2NEt / CH₂Cl₂

6.1: 100 percent / NaBH₄ / methanol

7.1: 100 percent / (i-Pr)2NEt / CH₂Cl₂

With methanol; sodium tetrahydroborate; n-butyllithium; formic acid; ammonium cerium(IV) nitrate; N-ethyl-N,N-diisopropylamine; silver(l) oxide; palladium; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; acetonitrile;
DOI:10.1016/S0040-4039(02)02743-0

Reference yield:

: 603127-06-6
(2S,3R,4S)-3,4-Bis-benzyloxy-2-((S)-11-methoxymethoxy-13-methyl-tetradec-1-ynyl)-5-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester

: 603127-09-9
[(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / HCOOH; methanol / Pd

2: 74 percent / Ag₂O / ethyl acetate

3: 100 percent / (i-Pr)2NEt / CH₂Cl₂

4: 100 percent / NaBH₄ / methanol

5: 100 percent / (i-Pr)2NEt / CH₂Cl₂

With methanol; sodium tetrahydroborate; formic acid; N-ethyl-N,N-diisopropylamine; silver(l) oxide; palladium; In methanol; dichloromethane; ethyl acetate;
DOI:10.1016/S0040-4039(02)02743-0