HuagongsheHuagongshe Chemistry Print Report · For research reference only
Neopentyl glycol → HCID 58294023, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Neopentyl glycol | HCID 31344 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 58294044 | HCID 58294044 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58294023 | HCID 58294023 | 63% |
Reaction Steps
A solution of 3′-bromo-2′-(2-bromoethoxy)-5′-chloroacetophenone (Reference compound No. 4-1, 4.4 g, 10 mmol), neopentylglycol (1.2 g, 1.2 mmol) and p-toluenesulfonic acid monohydrate (0.22 g, 12 mmol) in anhydrous toluene (50 mL) was refluxed overnight. After cooling, ethyl acetate (50 mL) and saturated aqueous sodium hydrogen carbonate solution (100 mL) were added to the reaction mixture and the whole was partitioned. The organic layer was washed with brine (50 mL) and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give the title reference compound (2.8 g) as a pale yellow oil (Yield 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088817B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-1e722cd6cb864abaadc7dd172d27a866 |
| Source note | uspto-grants-2012_01 |