HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272796Generated: October 26, 2026
Water → O-(2-methoxybenzyl)-6-dimethylaminohexanol
https://huagongshe.com/reaction/272796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Dimethylaminohexan-1-ol | HCID 74623 | — |
| Reactant | 2-(Chloromethyl)anisole | HCID 81495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | O-(2-methoxybenzyl)-6-dimethylaminohexanol | HCID 23436782 | — |
Reaction Steps
6-(Dimethylamino)hexanol (8.80 g, 60.6 mmol) was dissolved in an anhydrous 2:1 mixture of tetrahydrofuran and dimethylfornamide (150 mL) and the solution was cooled in an ice bath. Sodium hydride (60% in oil, 3.23 g, 80.8 mmol) was added in portions and after 5 min. the water bath was removed. After 45 min., 2-methoxybenzyl chloride (6.28 g, 40.4 mmol) was added. After 4 h, the reaction mixture was quenched with 1 M sodium thiosulfate and tetrahydrofuran was removed in vacuo. The reaction mixture was washed with ethyl acetate and the aqueous phase was basified with 3 M sodium hydroxide, followed by extraction with ether. The ether layer was dried over potassium carbonate, filtered and acidified with 4 M hydrochloric acid in dioxane. The reaction mixture was concentrated in vacuo and the residue was crystallized form ethanol/ether to give O-(2-methoxybenzyl)-6-dimethylaminohexanol as the hydrochloride salt (10.4 g, 85%). MS (M-Cl)+266.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456203B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-6aff08e24c004d02b3a693f66a0b9f8b |
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| Source note | uspto-grants-2008_11 |
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