[(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester

Base Information

Chemical Name:[(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester
CAS No.:208193-02-6
Molecular Formula:C₂₅H₃₉NO₆Si
Molecular Weight:477.673
Hs Code.:

Synonyms:[(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester

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Chemical Property of [(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester

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Technology Process of [(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester

There total 10 articles about [(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl 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: 49.0%

: 79-22-1
methyl chloroformate

: (R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enylamine

: 208193-02-6
[(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester

Guidance literature:: In pyridine; dichloromethane; at 0 ℃; for 1.5h;
DOI:10.1016/S0040-4020(98)00975-2

Reference yield:

: 4746-97-8
cyclohexanedione monoethylene ketal

: 208193-02-6
[(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 1.) n-BuLi / 1.) THF, 2.) THF

2: POCl₃, DBU, pyridine

3: H₂ / Pd/C

4: H₃O⁽¹⁺⁾, MeOH

5: lithium (+)-bis(α-methylbenzyl)amide, LiCl / tetrahydrofuran / -78 °C

6: TMSN₃, (PhIO)n / CH₂Cl₂ / -15 °C

7: LiAlH₄ / diethyl ether

8: pyridine

With pyridine; methanol; lithium aluminium tetrahydride; n-butyllithium; trimethylsilylazide; (+)-bis(α-methylbenzyl)amine lithium salt; (PhIO)n; oxonium; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/ja980407s

Reference yield:

: 91511-83-0
5-bromo-7-methoxy-1,3-benzodioxol

: 208193-02-6
[(1R,6R)-6-(7-Methoxy-benzo[1,3]dioxol-5-yl)-3-triisopropylsilanyloxy-cyclohex-2-enyl]-carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 1.) n-BuLi / 1.) THF, 2.) THF

2: POCl₃, DBU, pyridine

3: H₂ / Pd/C

4: H₃O⁽¹⁺⁾, MeOH

5: lithium (+)-bis(α-methylbenzyl)amide, LiCl / tetrahydrofuran / -78 °C

6: TMSN₃, (PhIO)n / CH₂Cl₂ / -15 °C

7: LiAlH₄ / diethyl ether

8: pyridine

With pyridine; methanol; lithium aluminium tetrahydride; n-butyllithium; trimethylsilylazide; (+)-bis(α-methylbenzyl)amine lithium salt; (PhIO)n; oxonium; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/ja980407s