HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-Chloro-4-methoxybenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Chloro-p-anisic acid | HCID 169982 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Chloro-4-methoxybenzoyl chloride | HCID 4769299 | — |
Reaction Steps
A stirred solution of 0.22 gram (0.0012 mole) of 3-chloro-4-methoxybenzoic acid in a small amount of tetrahydrofuran and chloroform was cooled to 0° C., and 0.12 mL (0.0014 mole) of oxalyl chloride was added dropwise. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature, where it was stirred for about 3.5 hours. After this time the reaction mixture was concentrated under reduced pressure, yielding 3-chloro-4-methoxybenzoyl chloride, which was dissolved in a small amount of tetrahydrofuran for later use.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05569664 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-ef7b2c9f6f784ede8ceb8024279c9555 |
| Source note | uspto-grants-1996_10 |