HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274346Generated: October 30, 2026
4-Hydroxybenzaldehyde → HCID 86645079, compound
https://huagongshe.com/reaction/2274346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(3-Chlorophenyl)oxirane | HCID 155613 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86645079 | HCID 86645079 | 10% |
Reaction Steps
To a stirring solution of 2-(3-chlorophenyl)oxirane (6.20 g, 40.0 mmol) in toluene (65 mL) was added 4-hydroxybenzaldehyde (7.30 g, 60.0 mmol), 1M NaOH (65 mL) and PEG4000 (polyethylene glycol, 0.85 g) and the stirring mixture was heated at 78° C. for three hours. The reaction was allowed to cool to RT and then extracted with EtOAc (2×150 mL). The combined extracts were washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The resulting light brown oil was adsorbed onto silica gel and chromatographed eluting with 25-40% EtOAc/hexanes. There are 2 major spots. Fractions containing the higher Rf spot were combined and evaporated in vacuo to give 1.08 g (10%) of the desired product as a colorless oil. Fractions containing the lower Rf spot were combined and evaporated in vauo to give 0.95 g (8%) of the regioisomer as a colorless oil, 44B. Some starting epoxide (2.85 g) was also recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09126959B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-0681bbc3b5c5485888b814f8746367b9 |
|---|
| Source note | uspto-grants-2015_09 |
|---|