HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyraldehyde → HCID 53840005, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-1-(chloromethyl)-4-fluorobenzene | HCID 2725064 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53840005 | HCID 53840005 | 57.9% |
Reaction Steps
65.0 g of 2-chloro-4-fluorobenzyl chloride in 90 ml of toluene and 28.8 g of isobutyraldehyde are added dropwise, simultaneously but separately, with thorough mixing at 80° C. in the course of 30 minutes to a mixture of 1.9 g of tetrabutylammonium iodide, 155 g of 30% strength sodium hydroxide solution and 115 ml of toluene, and stirring is continued for 3 hours at 80° C. The organic phase is separated off, washed with three times 50 ml of water, dried, and concentrated (58.5 g) by short-path distillation (bp.=70°-90° C./0.3). Distillation gives 45.1 g of (2-chloro-4-fluorophenyl)-pivalaldehyde (bp.: 53°-55° C./0.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05013354 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-2addd1b5522a467699a2191e4079b320 |
| Source note | uspto-grants-1991_05 |