HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 63433147, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 61088367 | HCID 61088367 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 63433147 | HCID 63433147 | 97% |
Reaction Steps
To a solution of 1-benzothiophen-3-yl(cyclohexyl)methanol (2.32 g) synthesized above in toluene (25 mL) was added dropwise thionyl chloride (824 μL), and the mixture was stirred at room temperature for 4 hr. The reaction mixture was poured into ice-cooled saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give the title object compound (2.42 g, 97%) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-e4e6a3b29b8a437bb83dccbd08cf9259 |
| Source note | uspto-grants-2013_05 |