HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Oxide → 3-Benzenesulfonyl-3-methyl-butan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | ((1-Methylethyl)sulfonyl)benzene | HCID 199476 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Benzenesulfonyl-3-methyl-butan-1-ol | HCID 14906979 | 99% |
Reaction Conditions
| Temperature | -40 °C |
|---|
Reaction Steps
A solution of n-butyllithium in cyclohexanes (1.8M, 35.1 ml; 63.18 mmol) was added dropwise to a stirred solution of isopropyl phenyl sulphone (9.95 g, 54 mmol) in tetrahydrofuran (100 ml) keeping the temperature of the mixture below −60° C. The mixture was stirred for 30 min. and ethylene oxide was passed through the reaction mixture for 10 min. The mixture was warmed up to −40° C. for 30 min., then quenched with sat. aqueous NH4Cl and extracted into ethyl acetate. The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified on silica gel (i-hexane:ethyl acetate) to give the title compound (12.3 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101892B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-f8737e092ee344178f600929b7151bbd |
| Source note | uspto-grants-2006_09 |