HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → HCID 19105433, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | HCID 19105436 | HCID 19105436 | — |
| Product | HCID 19105433 | HCID 19105433 | 83% |
Reaction Steps
A mixture of p-hydroxymethylbenzyl vinylbenzyl ether (39.2 g, 0.16 molar), triphenylphosphine (46.0 g, 0.18 molar), and 2,6-di-tert-butyl-p-cresol (0.5 g) in carbon tetrachloride (550 ml) was heated at reflux for 2 hours and then stirred at ambient temperature overnight. The next day the reaction was filtered and the solvent removed on a rotary evaporator. To the residue was added methanol (300 ml) to precipitate a white solid: m.p. of 110°-112° C. Yield of 83%. Analysis calculated for C16H15C10: C, 74.27, H, 5.84. Found: C, 73.15, H, 5.84. 1H NMR (CDCl3) δ 4.5)s. 2H, CH2Cl), 5.0 (s, 2H, CH2O), 5.2+5.75 (AB quartet, 2H, CH2 =), 6.75 (m, 1H, CH=), 6.9+7.3 (AB quartet, 4H, ##STR22## 7.4 (s, 4H, ##STR23##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05278267 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-03fefd6d10714b6d918bb2a13e2fd1ea |
| Source note | uspto-grants-1994_01 |