HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069031Generated: October 29, 2026
Ammonium Chloride → 1-Phenoxy-3-vinylbenzene
https://huagongshe.com/reaction/1069031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Triphenylmethyl phosphonium bromide | HCID 21951224 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenoxy-3-vinylbenzene | HCID 9837041 | 71.9% |
Reaction Steps
A suspension of triphenylmethylphosphonium bromide (25.23 g) and potassium tert-butoxide (1M solution in tetrahydrofuran) (75.67 ml) was stirred at 0° C. for 0.5 h. A solution of 3-phenoxy-benzaldehyde (10.0 g) in THF (10 ml) was added to the mixture and the reaction mixture stirred at 0° C. for 4 h. Ammonium chloride solution was added and the mixture extracted with diethyl ether. The organic extracts were combined, washed with water, dried and concentrated. Purification (SiO2, isohexane:ethyl acetate 4:1 as eluant) gave the subtitle compound (7.12 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06251910B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-be9fb439323f43619c9e52c210405015 |
|---|
| Source note | uspto-grants-2001_06 |
|---|