HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 18913738, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 22374130 | HCID 22374130 | — |
| Reactant | HCID 53922221 | HCID 53922221 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18913738 | HCID 18913738 | — |
Reaction Steps
Preparation of 3,5-difluoro-4-cyanophenyl 4'-(pentyloxymethyl)biphenyl-4-carboxylate (in the formula (1), R=C5 H11, l=1, m and n=both, 1, o=0, A1 and A2 =both, 1,4-phenylene group, Z1 =covalent bond, Z2 =--COO--, X=CN, and Y1 and Y2 =both, F) (Compound No. 229) 4'-(Pentyloxymethyl)biphenyl-4-carboxyic acid (2.1 g, 7.0 mmol) was mixed with thionyl chloride (1.3 g, 10.6 mmol), pyridine (0.1 ml) and toluene (4 ml), followed by reacting them at 80° C. for 2 hours, and distilling off superfluous thionyl chloride and toluene under reduced pressure, to obtain raw 4'-(pentyloxymethyl)biphenyl-4-carbonyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05755994 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-ba2cd864e5874b0ea3d57a7670c063a2 |
| Source note | uspto-grants-1998_05 |