(+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

Base Information

Chemical Name:(+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester
CAS No.:129657-91-6
Molecular Formula:C₃₀H₄₃O₇P
Molecular Weight:546.641
Hs Code.:

(+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzo<b,d>pyran-4-yl>phosphonic acid diethyl ester

Synonyms:(+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

Suppliers and Price of (+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

There total 11 articles about (+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl 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: 62.0%

: 129658-02-2
[(6aR,9R,10aR)-1,9-Bis-benzyloxy-6,6-dimethyl-3-((S)-1-methyl-4-phenyl-butoxy)-6a,7,8,9,10,10a-hexahydro-6H-benzo[c]chromen-4-yl]-phosphonic acid diethyl ester

: 129657-91-6
(+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 4.5h; under 760 Torr;
DOI:10.1002/jhet.5570270312

Reference yield:

: 63790-07-8
1-methyl-4-phenylbutyl methanesulphonate

: 129657-91-6
(+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: K₂CO₃ / dimethylformamide / 80 °C

2: NaH / diethyl ether / 18 h

3: Et₃N / methanol / 20 h / 25 °C

4: 54 percent / KOH / ethanol / 18 h / Heating

5: 3 percent / Li, liq. NH₃ / tetrahydrofuran / -78 °C

6: 1) KH / 1) DMF, 25 deg C, 30 min, 2) 9 h, 25 deg C

7: N-bromosuccinimide / CCl₄ / 1) 0 deg C, 2 h, 2) 25 deg C

8: n-butyllithium / 1) THF, -78 deg C, 1 h, 2) -78 deg C, 5 min

9: 62 percent / H₂ / Pd/C / methanol / 4.5 h / 760 Torr

With potassium hydroxide; N-Bromosuccinimide; n-butyllithium; ammonia; hydrogen; lithium; potassium hydride; sodium hydride; potassium carbonate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; tetrachloromethane; diethyl ether; ethanol; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570270312

Reference yield:

: 63789-85-5
2,3-dihydro-2,2-dimethyl-5-hydroxy-7-(1-methyl-4-phenylbutoxy)-4H-1-benzopyran-4-one

: 129657-91-6
(+/-)-<6aβ,7,8,9,10,10aα-hexahydro-1,9β-dihydroxy-6,6-dimethyl-3-(1-methyl-4-phenylbutoxy)-6H-dibenzopyran-4-yl>phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: NaH / diethyl ether / 18 h

2: Et₃N / methanol / 20 h / 25 °C

3: 54 percent / KOH / ethanol / 18 h / Heating

4: 3 percent / Li, liq. NH₃ / tetrahydrofuran / -78 °C

5: 1) KH / 1) DMF, 25 deg C, 30 min, 2) 9 h, 25 deg C

6: N-bromosuccinimide / CCl₄ / 1) 0 deg C, 2 h, 2) 25 deg C

7: n-butyllithium / 1) THF, -78 deg C, 1 h, 2) -78 deg C, 5 min

8: 62 percent / H₂ / Pd/C / methanol / 4.5 h / 760 Torr

With potassium hydroxide; N-Bromosuccinimide; n-butyllithium; ammonia; hydrogen; lithium; potassium hydride; sodium hydride; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; tetrachloromethane; diethyl ether; ethanol;
DOI:10.1002/jhet.5570270312