(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 4-methoxyphenyl ester

Base Information

Chemical Name:(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 4-methoxyphenyl ester
CAS No.:769950-28-9
Molecular Formula:C₃₃H₄₆O₈S
Molecular Weight:602.789
Hs Code.:

(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 4-methoxyphenyl ester

Synonyms:(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 4-methoxyphenyl ester

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Chemical Property of (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 4-methoxyphenyl ester

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Technology Process of (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 4-methoxyphenyl ester

There total 4 articles about (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 4-methoxyphenyl 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: 54.3%

: 150-76-5
4-methoxy-phenol

: (20E)-3-O-(methylsulfonyl)-22-secoebelin-22-al lactone

: 769950-28-9
(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 4-methoxyphenyl ester

Guidance literature:: (20E)-3-O-(methylsulfonyl)-22-secoebelin-22-al lactone; With N-Bromosuccinimide; In tetrachloromethane; for 0.0833333h; Irradiation;

4-methoxy-phenol; With triethylamine; In tetrachloromethane; at 20 ℃; for 1h;
DOI:10.1002/hlca.200490163

Reference yield:

: 54815-36-0
jujubogenin

: 769950-28-9
(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 4-methoxyphenyl ester

Guidance literature:: Multi-step reaction with 4 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: 54.3 percent / Et₃N / CCl₄ / 1 h / 20 °C

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

Reference yield:

: (1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-2'-[(1EZ,3E)-2,6-dimethylhepta-1,3,5-trienyl]dodecahydro-7'-hydroxy-4'b,8',8',10'a-tetramethylspiro[furan-3(2H),1'(2'H)-phenanthren]-5(4H)-one

: 769950-28-9
(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 4-methoxyphenyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / 10 h / 0 °C

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

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

3.1: NBS / CCl₄ / 0.08 h / Irradiation

3.2: 54.3 percent / Et₃N / CCl₄ / 1 h / 20 °C

With pyridine; N-Bromosuccinimide; ozone; In methanol; tetrachloromethane; dichloromethane;
DOI:10.1002/hlca.200490163