5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester

Base Information

Chemical Name:5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester
CAS No.:139897-32-8
Molecular Formula:C₃₉H₄₂O₇SeSi
Molecular Weight:729.804
Hs Code.:

5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester

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Chemical Property of 5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester

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Technology Process of 5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester

There total 9 articles about 5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic 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: 97.0%

: 139897-31-7
5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-(phenylselanyl-phenylsulfanyl-methyl)-furan-3-carboxylic acid methyl ester

: 139897-32-8,139913-91-0
5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester

Guidance literature:: With silver perchlorate; In water; benzene;

Reference yield:

: 126822-71-7
1-iodo-2-<(tert-butyldiphenylsilyl)oxy>ethane

: 139897-32-8,139913-91-0
5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) lithium diisopropylamide, 2.) 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidone (DMPU) / 1.) THF, -78 deg C, 45 min, 2.) THF, a) -78 deg C, 30 min, b) RT, 18 h

2: 1.) lithium diisopropylamide / 1.) hexane, THF, -78 deg C, 45 min, 2.) hexane, THF, -78 deg C, 1 h

3: 1.) ozone, 2.) PPh₃ / 1.) CH₂Cl₂, -78 deg C, 10 min, 2.) CH₂Cl₂, RT, 5 h

4: 86 percent / BF₃*OEt₂ / CH₂Cl₂ / 0.17 h / -78 °C

5: 90 percent / 10-camphorsulfonic acid / benzene / Heating

6: 1.) potassium hexamethyldisilazide / 1.) THF, toluene, -78 deg C, 40 min, 2.) THF, toluene, -78 deg C, 1 h

7: 97 percent / silver perchlorate / benzene; H₂O

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; boron trifluoride diethyl etherate; (1S)-10-camphorsulfonic acid; silver perchlorate; potassium hexamethylsilazane; ozone; triphenylphosphine; lithium diisopropyl amide; In dichloromethane; water; benzene;

Reference yield:

: 139897-19-1
(2-bromoethoxy)(tert-butyl)diphenylsilane

: 139897-32-8,139913-91-0
5-((R)-1-{(R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-oxo-4-phenylselanyl-tetrahydro-furan-2-yl}-2-methyl-allyl)-2-formyl-furan-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 95 percent / sodium iodide / acetone / 36 h / Ambient temperature

2: 1.) lithium diisopropylamide, 2.) 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidone (DMPU) / 1.) THF, -78 deg C, 45 min, 2.) THF, a) -78 deg C, 30 min, b) RT, 18 h

3: 1.) lithium diisopropylamide / 1.) hexane, THF, -78 deg C, 45 min, 2.) hexane, THF, -78 deg C, 1 h

4: 1.) ozone, 2.) PPh₃ / 1.) CH₂Cl₂, -78 deg C, 10 min, 2.) CH₂Cl₂, RT, 5 h

5: 86 percent / BF₃*OEt₂ / CH₂Cl₂ / 0.17 h / -78 °C

6: 90 percent / 10-camphorsulfonic acid / benzene / Heating

7: 1.) potassium hexamethyldisilazide / 1.) THF, toluene, -78 deg C, 40 min, 2.) THF, toluene, -78 deg C, 1 h

8: 97 percent / silver perchlorate / benzene; H₂O

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; boron trifluoride diethyl etherate; (1S)-10-camphorsulfonic acid; silver perchlorate; potassium hexamethylsilazane; ozone; triphenylphosphine; sodium iodide; lithium diisopropyl amide; In dichloromethane; water; acetone; benzene;