HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20360684, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | Methanone, (4-nitrophenyl)phenyl- | HCID 70839 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20360684 | HCID 20360684 | 91% |
Reaction Steps
Acetylene is introduced for 30 minutes into a 20°-22° C mixture of 118 ml. of tetrahydrofuran and 16.8 g. of potassium-tert.butylate, and thereafter 22.7 g. of 4-nitro-benzophenone are added to the mixture. The introduction of acetylene is continued at 20° to 22° C for an additional 30 minutes, then the mixture is neutralized with 5 n hydrochloric acid under nitrogen atmosphere. The organic phase is separated, dried over anhydrous sodium sulfate, and the solvent is distilled off in vacuo. 23.1 g. (91%) of 4-nitro-α-ethynyl-benzhydrol are obtained; m.p.: 88°-89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04066709 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-b55a5740adcb4a9dbc517fab90b657b4 |
| Source note | uspto-grants-1978_01 |