HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 70415731, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Hydroxy-3-methylbut-1-yl-diphenylphosphine oxide | HCID 21291216 | — |
| Reactant | HCID 178527022 | HCID 178527022 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 70415731 | HCID 70415731 | — |
Reaction Steps
The phosphine oxide from (f) above (1.4 g) was dissolved in dihydripyran (20 ml) and benzene (5 ml). p-Toluenesulphonic acid (10 mg) was added. After 20 hr, the mixture was concentrated, added to CH2Cl2 and washed with 5% aqueous NaHCO3 /brine and dried. Evaporation of the solvent gave the crude product (1.8 g) essentially quantitatively as a solid. Recrystallised from acetone. m.p. 146°-148° C.; 1Hnmr δ 8.0-7.3 (m, 10 H, aryl), 4.67 (m, W=6 Hz, THP, C-2'H), 3.67 (m, W=36 Hz, THP, C-6'H2), 1.23 (s, 6H); IR νmax 2950 (m), 1440 (m), 118C (s), cm-1 ; (analysis found: % C, 70.80; H, 7.73; P, 8.54; C22H29O3P requires % C, 70.96; H, 7.85; P, 8.32.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04772433 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-641e3e0d32f7400488d3f4f8219356d7 |
| Source note | uspto-grants-1988_09 |