HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylbenzaldehyde → 1-(Biphenyl-3-ylmethyl)-4-(2-chlorophenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylbenzaldehyde | HCID 121053 | — |
| Reactant | 1-(2-Chlorophenyl)piperazinium chloride | HCID 3017015 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-(Biphenyl-2-ylmethyl)-4-phenylpiperazine | HCID 71602523 | — |
| Product | 1-(Biphenyl-3-ylmethyl)-4-(2-chlorophenyl)piperazine | HCID 71678508 | — |
Reaction Steps
200.0 mg of the target compound (0.55 mmol, 67.2%) was obtained using 1-(2-chlorophenyl)piperazine hydrochloride (382 mg, 1.64 mmol), biphenyl-3-carbaldehyde (150 mg, 0.82 mmol) and NaBH(OAc)3 (529 mg, 2.46 mmol) according to the synthesis method of Compound 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883796B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-ba057476627d44eca0a2947951c40bc1 |
| Source note | uspto-grants-2014_11 |