C₁₇H₂₁F₃O₆S

Base Information

Chemical Name:C₁₇H₂₁F₃O₆S
CAS No.:1056681-24-3
Molecular Formula:C₁₇H₂₁F₃O₆S
Molecular Weight:410.411
Hs Code.:

C<sub>17</sub>H<sub>21</sub>F<sub>3</sub>O<sub>6</sub>S

Synonyms:C₁₇H₂₁F₃O₆S

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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 C₁₇H₂₁F₃O₆S

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Technology Process of C₁₇H₂₁F₃O₆S

There total 9 articles about C₁₇H₂₁F₃O₆S 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:

: 358-23-6
trifluoromethylsulfonic anhydride

: 1056674-54-4
(3S,5S)-5-[(1R)-2-(benzyloxy)-1-hydroxyethyl]-3-isopropyldihydrofuran-2(3H)-one

: 1056681-24-3
C₁₇H₂₁F₃O₆S

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃; for 0.25 - 0.5h; Product distribution / selectivity;

Reference yield:

: 1056674-35-1
5,6-di-O-benzyl-2,3-dideoxy-D-glucono-1,4-lactone

: 1056681-24-3
C₁₇H₂₁F₃O₆S

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran; tris(pyrrolidino)phosphine oxide / -60 °C

2.1: hydrogen / palladium 10% on activated carbon / methanol / 2250.23 Torr

3.1: di(n-butyl)tin oxide / toluene / 4 h / Heating / reflux

3.2: 22 h / 90 °C

4.1: pyridine / dichloromethane / 0.25 - 0.5 h / 0 - 20 °C

With pyridine; hydrogen; di(n-butyl)tin oxide; lithium diisopropyl amide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; tris(pyrrolidino)phosphine oxide; toluene;

Reference yield:

: 1056674-18-0
methyl 5,6-di-O-benzyl-3-deoxy-α-D-glucofuranoside

: 1056681-24-3
C₁₇H₂₁F₃O₆S

Guidance literature:: Multi-step reaction with 7 steps

1.1: tetrahydrofuran / 2 h / Heating / reflux

2.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 0.33 h / 100 °C

3.1: boron trifluoride diethyl etherate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 17 h / 0 - 20 °C

4.1: lithium diisopropyl amide / tetrahydrofuran; tris(pyrrolidino)phosphine oxide / -60 °C

5.1: hydrogen / palladium 10% on activated carbon / methanol / 2250.23 Torr

6.1: di(n-butyl)tin oxide / toluene / 4 h / Heating / reflux

6.2: 22 h / 90 °C

7.1: pyridine / dichloromethane / 0.25 - 0.5 h / 0 - 20 °C

With pyridine; 2,2'-azobis(isobutyronitrile); boron trifluoride diethyl etherate; hydrogen; tri-n-butyl-tin hydride; di(n-butyl)tin oxide; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; tris(pyrrolidino)phosphine oxide; toluene;