(2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

Base Information

Chemical Name:(2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester
CAS No.:769950-35-8
Molecular Formula:C₃₄H₄₆O₇
Molecular Weight:566.735
Hs Code.:

(2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

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Suppliers and Price of (2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

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Chemical Property of (2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

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Technology Process of (2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

There total 6 articles about (2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl 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: 27.6%

: 769950-30-3
(2E)-2-methyl-3-[(1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]prop-2-enoic acid 3,4,5-trimethoxyphenyl ester

: 769950-35-8
(2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

Guidance literature:: With lithium carbonate; In N,N-dimethyl acetamide; for 0.5h; Heating;
DOI:10.1002/hlca.200490163

Reference yield:

: 642-71-7
3,4,5-trimethoxyphenol

: 769950-35-8
(2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: NBS / CCl₄ / 0.08 h / Irradiation

1.2: 21.1 percent / Et₃N / CCl₄ / 1 h / 20 °C

2.1: 27.6 percent / Li₂CO₃ / N,N-dimethyl-acetamide / 0.5 h / Heating

With N-Bromosuccinimide; lithium carbonate; In tetrachloromethane; N,N-dimethyl acetamide;
DOI:10.1002/hlca.200490163

Reference yield:

: 54815-36-0
jujubogenin

: 769950-35-8
(2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: HCl / ethanol; H₂O / 5 h / 80 °C

2.1: pyridine / 10 h / 0 °C

3.1: O₃ / CH₂Cl₂; methanol / 1 h / -78 °C

3.2: Me₂S / CH₂Cl₂; methanol / 2 h / -10 - 0 °C

4.1: NBS / CCl₄ / 0.08 h / Irradiation

4.2: 21.1 percent / Et₃N / CCl₄ / 1 h / 20 °C

5.1: 27.6 percent / Li₂CO₃ / N,N-dimethyl-acetamide / 0.5 h / Heating

With pyridine; hydrogenchloride; N-Bromosuccinimide; lithium carbonate; ozone; In methanol; tetrachloromethane; ethanol; dichloromethane; N,N-dimethyl acetamide; water;
DOI:10.1002/hlca.200490163