HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178467882, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178467883 | HCID 178467883 | — |
| Reactant | HCID 178467884 | HCID 178467884 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178467882 | HCID 178467882 | — |
Reaction Steps
Preparation of 3,5-difluoro-4-cyanophenyl 4-(trans-4-(ethoxymethyl)cyclohexyl)benzoate (in the formula (1), R=C2H5, l=1, m and n=both, 1, o=0, A1 =trans-1,4-cyclohexylene group, A2 =1,4-phenylene group, Z1 =covalent bond, Z2 =--COO--, X=CN, and Y1 and Y2 =both, F) (Compound No. 187) 4-(Trans-4-(ethoxymethyl)cyclohexyl)benzoic acid (1.9 g, 7.1 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-(trans-4-(ethoxymethyl)cyclohexyl)benzoyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05755994 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-e77d97afa2a74a6ca45209498679ce3d |
| Source note | uspto-grants-1998_05 |