HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 3',4',5'-Trimethoxy-biphenyl-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3',4',5'-Trimethoxy-biphenyl-2-carboxylic acid | HCID 59785704 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3',4',5'-Trimethoxy-biphenyl-2-carbonyl chloride | HCID 16116289 | — |
Reaction Steps
(The following reaction is done in an anhydrous N2 atmosphere.) Dissolve 3′,4′,5′-Trimethoxy-biphenyl-2-carboxylic acid (56) (54 mg, 0.18 mmol) in anhydrous DCM (1.3 mL) and add anhydrous DMF (1 drop, cat. amount). Then add slowly oxalyl chloride (21 μL, 0.24 mmol) by keeping temperature at ca. 20° C. with a water bath and stir the turbid mixture for additional 2 h at it Remove solvent and dry in vacuum to obtain crude 3′,4′,5′-Trimethoxy-biphenyl-2-carbonyl chloride (57) as a yellow solid. No further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394835B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-19b24ddd10014d24a39941fc8d1f30e9 |
| Source note | uspto-grants-2013_03 |