HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841126Generated: October 31, 2026
p-Toluenesulfonic acid → HCID 86757942, compound
https://huagongshe.com/reaction/841126
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | 4-Bromo-2-fluorophenol | HCID 2724981 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86757942 | HCID 86757942 | — |
Reaction Steps
p-Toluene sulfonic acid (0.40 g) was added to an ice-cooled solution of 4-Bromo-2-fluoro phenol (205.38, 1.075 mol) in dihydro-2H-pyran (452.23 g, 5.376 moles). The ice bath was removed after 30 min. and the mixture was stirred for two hours and then diluted with methylene chloride (500 ml). The methylene chloride solution was extracted with 10% aqueous KOH solution (3×500 ml), rinsed with water (3×500 ml), dried over MgSO4, filtered and rotavaped. The crude product was further dried overnight over a vacuum pump and then vacuum distilled. The first distillation fraction was unreacted phenol, (52.0 g) followed by a fraction of the protected phenol (212.29 g, 71.8%). The purified product was frozen in dry ice/acetone bath and then allowed to sit in the refrigerator over 2-3 days to obtain the Monomer IA2 intermediate as clear needle shaped crystals, mp=25-27° C., mp of the Monomer IA1 intermediate=62-63° C., TLC (1:1CH2Cl2/hexane), Rf=0.42.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06369262B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-ae3ed61f2e724527abf1dd95b6aeb07d |
|---|
| Source note | uspto-grants-2002_04 |
|---|