{(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester

Base Information

Chemical Name:{(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester
CAS No.:221182-41-8
Molecular Formula:C₂₄H₃₁NO₅
Molecular Weight:413.514
Hs Code.:

Synonyms:{(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester

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Chemical Property of {(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester

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Technology Process of {(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester

There total 10 articles about {(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl 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:

: 501-53-1,94274-21-2
benzyl chloroformate

: (S)-1-[(1S,2S)-1-(4-Methoxy-benzyloxy)-2-triisopropylsilanyloxy-propyl]-1-methyl-but-3-enylamine

: 221182-41-8
{(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester

Guidance literature:: With water; sodium hydrogencarbonate; In 1,4-dioxane; at 23 ℃; for 2h; Yield given;
DOI:10.1002/(SICI)1521-3773(19990115)38:1/2<240::AID-ANIE240>3.0.CO;2-5

Reference yield:

: 221182-49-6
O-benzyl-N-{1-[1-(4-methoxy-benzyloxy)-2-triisopropylsilanyloxy-propyl]-1-methyl-but-3-enyl}-hydroxylamine

: 221182-41-8
{(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄ / diethyl ether / 5 h / Heating

2: aq. NaHCO₃ / dioxane / 18 h / 0 - 25 °C

With lithium aluminium tetrahydride; sodium hydrogencarbonate; In 1,4-dioxane; diethyl ether; 1: Substitution / 2: Acylation;
DOI:10.1002/(SICI)1521-3765(19990903)5:9<2648::AID-CHEM2648>3.0.CO;2-Q

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 221182-41-8
{(S)-1-[(1S,2S)-2-Hydroxy-1-(4-methoxy-benzyloxy)-propyl]-1-methyl-but-3-enyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / NaH / tetrahydrofuran / 3 h / 0 - 23 °C

2: LiAlH₄ / diethyl ether / 18 h / Heating

3: NaHCO₃, H₂O / dioxane / 2 h / 23 °C

With lithium aluminium tetrahydride; water; sodium hydride; sodium hydrogencarbonate; In tetrahydrofuran; 1,4-dioxane; diethyl ether;
DOI:10.1002/(SICI)1521-3773(19990115)38:1/2<240::AID-ANIE240>3.0.CO;2-5