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(1R,3S,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(thymin-1-yl)-2,6-dioxabicyclo<3.2.1>octane

Base Information
  • Chemical Name:(1R,3S,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(thymin-1-yl)-2,6-dioxabicyclo<3.2.1>octane
  • CAS No.:229469-38-9
  • Molecular Formula:C21H24N2O7
  • Molecular Weight:416.431
  • Hs Code.:
(1R,3S,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(thymin-1-yl)-2,6-dioxabicyclo<3.2.1>octane

Synonyms:

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Chemical Property of (1R,3S,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(thymin-1-yl)-2,6-dioxabicyclo<3.2.1>octane
Chemical Property:
Purity/Quality:
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Technology Process of (1R,3S,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(thymin-1-yl)-2,6-dioxabicyclo<3.2.1>octane

There total 16 articles about (1R,3S,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(thymin-1-yl)-2,6-dioxabicyclo<3.2.1>octane 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:
Guidance literature:
Multi-step reaction with 16 steps
1: 1.) DCC, TFA, pyridine, 2.) oxalic acid / 1.) DMSO, Et2O, room temperature, 5 h, 2.) MeOH, room temperature, 1 h
2: 91 percent / sodium t-pentoxide / diethyl ether; benzene / 1.) room temperature, 6 h, 2.) -10 deg C, 1 h
3: 88 percent / TBAF / tetrahydrofuran / 1 h / Ambient temperature
4: pyridine / 15 h / Ambient temperature
5: 76 percent / NaH / tetrahydrofuran / 4 h / Ambient temperature
6: 1.) 9-BBN, 2.) sodium perborate tetrahydrate / 1.) room temperature, 1 h; 40 deg C, overnight, 2.) H2O, EtOH, 50 deg C, 4 h
7: pyridine / Ambient temperature
8: TBAF / tetrahydrofuran / 0.5 h / Ambient temperature
9: 90 percent / DCC, TFA, pyridine / dimethylsulfoxide / 1.) 10 deg C, 1 h, 2.) room temperature, 6 h
10: 94 percent / NaOH / H2O; dioxane / 48 h / Ambient temperature
11: pyridine / 0.75 h / Ambient temperature
12: AcOH / H2O / 2 h / Ambient temperature
13: NaH / tetrahydrofuran / 28 h / 55 °C
14: NaOH / H2O / 24 h / Heating
15: 99 percent / DMAP / CH2Cl2 / 2 h / Ambient temperature
16: 1.) ammonium sulfate, HMDS, 2.) SnCl4 / 1.) reflux, overnight, 2.) 1,2-dichloroethane, reflux, 2 h
With pyridine; dmap; sodium perborate; sodium hydroxide; ammonium sulfate; 9-borabicyclo[3.3.1]nonane dimer; tetrabutyl ammonium fluoride; oxalic acid; tin(IV) chloride; sodium tert-pentoxide; sodium hydride; acetic acid; dicyclohexyl-carbodiimide; 1,1,1,3,3,3-hexamethyl-disilazane; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; pyridine; diethyl ether; dichloromethane; water; dimethyl sulfoxide; benzene;
DOI:10.1016/S0040-4020(99)00394-4
Guidance literature:
Multi-step reaction with 17 steps
1: 88 percent / pyridine / 1.) 0 deg C, 1 h, 2.) room temperature, 1.5 h
2: 1.) DCC, TFA, pyridine, 2.) oxalic acid / 1.) DMSO, Et2O, room temperature, 5 h, 2.) MeOH, room temperature, 1 h
3: 91 percent / sodium t-pentoxide / diethyl ether; benzene / 1.) room temperature, 6 h, 2.) -10 deg C, 1 h
4: 88 percent / TBAF / tetrahydrofuran / 1 h / Ambient temperature
5: pyridine / 15 h / Ambient temperature
6: 76 percent / NaH / tetrahydrofuran / 4 h / Ambient temperature
7: 1.) 9-BBN, 2.) sodium perborate tetrahydrate / 1.) room temperature, 1 h; 40 deg C, overnight, 2.) H2O, EtOH, 50 deg C, 4 h
8: pyridine / Ambient temperature
9: TBAF / tetrahydrofuran / 0.5 h / Ambient temperature
10: 90 percent / DCC, TFA, pyridine / dimethylsulfoxide / 1.) 10 deg C, 1 h, 2.) room temperature, 6 h
11: 94 percent / NaOH / H2O; dioxane / 48 h / Ambient temperature
12: pyridine / 0.75 h / Ambient temperature
13: AcOH / H2O / 2 h / Ambient temperature
14: NaH / tetrahydrofuran / 28 h / 55 °C
15: NaOH / H2O / 24 h / Heating
16: 99 percent / DMAP / CH2Cl2 / 2 h / Ambient temperature
17: 1.) ammonium sulfate, HMDS, 2.) SnCl4 / 1.) reflux, overnight, 2.) 1,2-dichloroethane, reflux, 2 h
With pyridine; dmap; sodium perborate; sodium hydroxide; ammonium sulfate; 9-borabicyclo[3.3.1]nonane dimer; tetrabutyl ammonium fluoride; oxalic acid; tin(IV) chloride; sodium tert-pentoxide; sodium hydride; acetic acid; dicyclohexyl-carbodiimide; 1,1,1,3,3,3-hexamethyl-disilazane; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; pyridine; diethyl ether; dichloromethane; water; dimethyl sulfoxide; benzene;
DOI:10.1016/S0040-4020(99)00394-4
Guidance literature:
Multi-step reaction with 13 steps
1: pyridine / 15 h / Ambient temperature
2: 76 percent / NaH / tetrahydrofuran / 4 h / Ambient temperature
3: 1.) 9-BBN, 2.) sodium perborate tetrahydrate / 1.) room temperature, 1 h; 40 deg C, overnight, 2.) H2O, EtOH, 50 deg C, 4 h
4: pyridine / Ambient temperature
5: TBAF / tetrahydrofuran / 0.5 h / Ambient temperature
6: 90 percent / DCC, TFA, pyridine / dimethylsulfoxide / 1.) 10 deg C, 1 h, 2.) room temperature, 6 h
7: 94 percent / NaOH / H2O; dioxane / 48 h / Ambient temperature
8: pyridine / 0.75 h / Ambient temperature
9: AcOH / H2O / 2 h / Ambient temperature
10: NaH / tetrahydrofuran / 28 h / 55 °C
11: NaOH / H2O / 24 h / Heating
12: 99 percent / DMAP / CH2Cl2 / 2 h / Ambient temperature
13: 1.) ammonium sulfate, HMDS, 2.) SnCl4 / 1.) reflux, overnight, 2.) 1,2-dichloroethane, reflux, 2 h
With pyridine; dmap; sodium perborate; sodium hydroxide; ammonium sulfate; 9-borabicyclo[3.3.1]nonane dimer; tetrabutyl ammonium fluoride; tin(IV) chloride; sodium hydride; acetic acid; dicyclohexyl-carbodiimide; 1,1,1,3,3,3-hexamethyl-disilazane; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; pyridine; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1016/S0040-4020(99)00394-4
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