(1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

Base Information

Chemical Name:(1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester
CAS No.:769949-52-2
Molecular Formula:C₂₈H₃₅ClO₃S
Molecular Weight:487.103
Hs Code.:

(1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

Synonyms:(1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

Suppliers and Price of (1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

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Technology Process of (1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

There total 5 articles about (1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl 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: 63.2%

: 769949-78-2
(1'S,2'S,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)-phenanthrene]-2'-carbothioic acid S-(4-chlorophenyl) ester

: 769949-52-2
(1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

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

Reference yield:

: 54815-36-0
jujubogenin

: 769949-52-2
(1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl 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: 53.1 percent / Et₃N / CCl₄ / 1 h / 20 °C

5.1: 63.2 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

Reference yield:

: 318234-99-0
3-O-(methylsulfonyl)-20-secoebelin-20-al lactone

: 769949-52-2
(1'S,2'S,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'b,8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-4-chlorophenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: NBS / CCl₄ / 0.08 h / Irradiation

1.2: 53.1 percent / Et₃N / CCl₄ / 1 h / 20 °C

2.1: 63.2 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