HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349393Generated: November 1, 2026
4-Fluorobenzyl chloride → HCID 10236866, compound
https://huagongshe.com/reaction/1349393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | HCID 21093239 | HCID 21093239 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10236866 | HCID 10236866 | 54% |
Reaction Steps
2.00 g of 4-benzyl-4-dimethylaminocyclohexanol were dissolved in 20 ml of dimethylformamide; 1.06 g of potassium tert.-butoxide were added and stirring was carried out for 45 minutes, before 1.36 g of 4-fluorobenzyl chloride were added dropwise in the course of 30 minutes. After stirring overnight, the mixture was added to 25 ml of ice-water and extracted repeatedly with ethyl acetate. The combined extracts were washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated. The resulting crude product (2.78 g) was separated on silica gel with hexane/ethyl acetate (V:V=1:1). 1.58 g of [1-benzyl-4-(4-fluorobenzyloxy)cyclohexyl]dimethylamine were obtained and, as described for Example 1, were converted into 890 mg of the corresponding hydrochloride using chlorotrimethylsilane and water in 2-butanone (white solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07211694B2 |
|---|
| Source dataset | uspto-grants-2007_05 |
|---|
| ORD ID | ord-c5090b7786d24b038733342dab8f4abe |
|---|
| Source note | uspto-grants-2007_05 |
|---|