HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472899Generated: October 29, 2026
Hydrochloric Acid → HCID 62291536, compound
https://huagongshe.com/reaction/472899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 4-(Benzyloxy)-2-(chloromethyl)pyridine | HCID 12938559 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 62291536 | HCID 62291536 | — |
Reaction Steps
1.5 g (10.78 mmol) of hexamethylenetetramine and then 1.3 g of sodium iodide are added to 2.1 g (8.99 mmol) of 4-(benzyloxy)-2-(chloromethyl)pyridine (described in stage A) in 60 ml of dichloromethane. The reaction medium is heated at reflux for 12 hours and then concentrated under reduced pressure. The residue obtained is taken up in 45 ml of methanol. 7.5 ml (89.90 mmol) of a 12N hydrochloric acid solution are added. The reaction medium is heated at reflux for 16 hours. After addition of ethyl ether, the precipitate obtained is filtered off and then taken up in a saturated aqueous sodium carbonate solution. The aqueous phase is extracted with ethyl acetate, dried over sodium sulfate and then concentrated under reduced pressure. 1.1 g of a beige oil are collected. Mass spectrometry (ES+Mode): MH+=215
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633216B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-7032dbaac34b4c3c873ed494786a6918 |
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| Source note | uspto-grants-2014_01 |
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