HuagongsheHuagongshe Chemistry Print Report · For research reference only
Neopentyl glycol → 2-(4-Bromophenyl)-5,5-dimethyl-1,3-dioxane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Neopentyl glycol | HCID 31344 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(4-Bromophenyl)-5,5-dimethyl-1,3-dioxane | HCID 13714515 | 93% |
Reaction Steps
A mixture of 4-bromobenzaldehyde (100 g, 0.54 mole), neopentyl glycol (115 g, 1.10 mole), and p-toluenesulfonic acid (800 mg, 4 mmole) in benzene (800 mL) was heated to reflux using a Dean Stark apparatus for 16h. The reaction mixture was cooled to room temperature and most of the benzene was removed. The residue was partitioned between ethyl acetate (500 mL) and cold water (150 mL). The organic phase was washed with water (2×150 mL) and brine (1×150 mL), then dried (Na2SO4) and concentrated to give the desired product (136 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07605175B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-c4e7b5832ca3412f800b6b678a48024d |
| Source note | uspto-grants-2009_10 |