HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 15661440, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 15661438 | HCID 15661438 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 15661440 | HCID 15661440 | — |
Reaction Steps
Dichloromethane (5 ml) was cooled to -60° under N2, oxalyl chloride (1.65 ml, 1M solution in CH2Cl2, 1.1 eq) was added followed by DMSO (234 ml in 1 ml of CH2Cl2). The resulting solution was stirred at -60° for 10 min. The 3-bromo-1-acetoxymethyl-9-fluorenol (0.480 g) in a suspension of CH2Cl2 (2 ml) was added dropwise and the solution stirred at -60° for 0.5 hour. Et3N (1.06 ml) was added dropwise and the solution stirred at -60° for 15 minutes. The cooling bath was removed and water (5 ml) was added and the reaction mixture stirred at room temperature for 20 minutes. The organic phase was separated and the aqueous phase was extracted with EtOAc; the combined extract was dried without further purification in the next step. ##STR406##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05034384 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-3d72481d5230489792f7f1e108c1ccdb |
| Source note | uspto-grants-1991_07 |