HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 4-[2-(Diphenylmethoxy)ethyl]-1-[(4-iodophenyl)methyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Oxalate | HCID 71081 | — |
| Reactant | 4-Iodobenzyl bromide | HCID 954258 | — |
| Reactant | 4-(2-(Diphenylmethoxy)ethyl]piperidine | HCID 10732661 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[2-(Diphenylmethoxy)ethyl]-1-[(4-iodophenyl)methyl]piperidine | HCID 9914327 | — |
Reaction Steps
4-[2-(diphenylmethoxy)ethyl]piperidine (0.23 g, 0.77 mmol) was reacted with 4-iodo benzyl bromide (0.76 g, 2.5 mmol) and K2CO3 (1.00 g, 7 mmol) in EtOH (10 mL) to give a thick oil, 0.17 g (%). 1H NMR (300 MHz, CDCl3): 1.21-1.63 (7H, m), 1.87-1.93 (t, J=11 Hz, 2H, N(CH2)-), 2.79-2.83 (bd, J=12 Hz, 2H, N(CH2)-), 3.41-3.49 (4H, m), 5.31 (s, 1H, Ph2CHO-), 7.05-7.63 (14H, m, ArH). Free base was converted into its oxalate sale, m.p.=160-161° C. Anal. C27H30INO. (COOH)2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595331B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-75803d2883ba469dbb1ea485b939f594 |
| Source note | uspto-grants-2009_09 |