HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060762Generated: November 2, 2026
p-Toluenesulfonic acid monohydrate → HCID 57475766, compound
https://huagongshe.com/reaction/2060762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-(3-Bromophenyl)-tetrahydro-2H-pyran-4-ol | HCID 18996282 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57475766 | HCID 57475766 | 90% |
Reaction Steps
A mixture of 4-(3-bromophenyl)tetrahydro-2H-pyran-4-ol (11.17 g, 41.3 mmol) and p-toluenesulfonic acid monohydrate (0.797 g, 4.13 mmol) in toluene (100 mL) is heated to reflux for 30 minutes using a Dean-Stark trap to remove water. The reaction is diluted with water and 5 N NaOH and extracted with EtOAc. The organic layer is dried over Na2SO4 and the solvent is removed under reduced pressure to afford a residue that is purified on silica gel chromatography eluting with a linear gradient of 5% to 100% EtOAc in hexanes to give the title compound (8.85 g, 90%). 1H NMR (400 MHz, CDCl3) δ 2.45-2.50 (m, 2H), 3.92 (t, 2H, J=5.71 Hz), 4.31 (q, 2H, J=3.07 Hz, J=5.71 Hz), 6.12-6.14 (m, 1H), 7.19 (t, 1H, J=7.91 Hz), 7.28-7.32 (m, 1H), 7.36-7.39 (m, 1H), 7.51 (t, 1H, J=1.76 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08278441B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-8191954d7e094399a95d88a1138c9876 |
|---|
| Source note | uspto-grants-2012_10 |
|---|