HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226264Generated: October 26, 2026
4-Benzyloxybenzyl chloride → HCID 57754436, compound
https://huagongshe.com/reaction/226264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzyloxybenzyl chloride | HCID 70042 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 6,7-Difluoro-2-methylquinoline | HCID 22241377 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57754436 | HCID 57754436 | — |
Reaction Steps
A solution of 8.9 g (49.6 mmol) of the product from Example 1, step 3 in 90 ml THF is cooled at −50° C. 28.6 ml (57.2 mmol) of a 2M solution of lithium diisopropylamide are added and the solution is allowed to heat to −10° C. After 15′ stirring at this temperature the deep colored solution is again cooled to −50° C. A solution of 11.6 g (49.8 mmol) of 1-benzyloxy-4-chloromethyl-benzene in 60 ml THF is dropped into the cooled solution. The system is allowed to heat to room temperature and stirred overnight. The solvent is evaporated and the residue that solidifies on cooling is stirred with ethyl ether and filtered. The residue is filtered through SiO2 eluting with dichloromethane. The yield is 3.75 g (20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557212B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-ca395e8fb5b7438997f54e1087e83bcd |
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| Source note | uspto-grants-2009_07 |
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