HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 70937102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 68721249 | HCID 68721249 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70937102 | HCID 70937102 | — |
Reaction Steps
A 1M solution of TBAF (1.2 mL, 1.2 mmol) was neutralized with a drop of HOAc and added to a solution of 4-chloro-5-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-N-methyl-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-2-sulfonamide in THF (3 mL). The reaction mixture was stirred for 2 h at RT. Sat'd NaHCO3 was added and the aqueous phase was extracted with CH2Cl2. The combined organic phase was dried (Na2SO4), filtered, and evaporated to give 4-chloro-5-(hydroxymethyl)-N-methyl-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-2-sulfonamide as a light yellow oil that was used without purification and assumed to be quantitative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-70ba431f8ae9458c9f62ea7a00f33b79 |
| Source note | uspto-grants-2012_11 |