HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl phenylmalonate → Tetra-n-butyl ammonium diethylphenyl malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl phenylmalonate | HCID 66514 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tetra-n-butyl ammonium diethylphenyl malonate | HCID 86747399 | — |
Reaction Steps
To a three necked 100 mL round bottom flask fitted with a argon inlet, dropping funnel, distillation unit and magnetic needle, was added 7.7 mmoles of tetrabutylammonium hydroxide (20% solution in toluene/methanol) in 40 mL of dry toluene and heated to +75° C. to +85° C. Diethylphenylmalonate (9.3 mmoles) was slowly added. Simultaneously an azeotrope of toluene-water was distilled out slowly over a period of 3 hours. After all toluene had distilled over, the flask was cooled to room temperature slowly. A solid product separated out, which was repeatedly washed with dry hexane. The initiator (tetra-n-butyl ammonium diethylphenyl malonate) thus formed was dried in vacuum and stored at room temperature under nitrogen or argon.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05266702 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-b91e56431fe24450a0867bd0ab3b335c |
| Source note | uspto-grants-1993_11 |