HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Formylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Product | 4-Formylbenzoyl chloride | HCID 12424620 | — |
Reaction Conditions
| Temperature | 2.5 °C |
|---|
Reaction Steps
To a thin suspension of 4-carboxybenzaldehyde (600 g, 3.92 mol) in tetrahydrofuran (2664 g, 36.57 mol) was added dimethylformadehyde (11.48 g, 0.16 mol) and the reaction mixture was cooled to 0-5° C. with an ice bath. The reaction mixture was then stirred at 0° C. while oxalyl chloride (608.69 g, 4.70 mol) was added slowly. The reaction mixture was stirred until it was deemed complete by 1HNMR to yield the title compound. The reaction mixture was used in the next step without further manipulation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728129B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-11c8be357cc7419c80cf8a2b182ca001 |
| Source note | uspto-grants-2010_06 |