HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275756Generated: October 31, 2026
Water → 3-(Cyclohexylmethoxy)pyridin-2-amine
https://huagongshe.com/reaction/2275756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Amino-3-Hydroxypyridine | HCID 28114 | — |
| Reactant | Cyclohexane, (bromomethyl)- | HCID 137636 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Cyclohexylmethoxy)pyridin-2-amine | HCID 13825890 | — |
Reaction Steps
At RT, 96 g of sodium hydroxide 45% strength in water (1081 mmol, 1 equivalent) were initially charged in 1170 ml of methanol, 119 g of 2-amino-3-hydroxypyridine (1080 mmol, 1 equivalent) were added and the mixture was stirred at RT for 10 min. The reaction mixture was concentrated under reduced pressure, the residue was taken up in 2900 ml of DMSO and 101 g of cyclohexylmethyl bromide (1135 mmol, 1.05 equivalents) were added. After 16 h at RT, the reaction mixture was added slowly to 6 l of water and the aqueous solution was extracted twice with in each case 21 of ethyl acetate. The combined organic phases were washed with in each case 1 l of saturated aqueous sodium bicarbonate solution and water, dried, filtered and concentrated. The residue was triturated with 500 ml of n-pentane, filtered and dried under reduced pressure. This gave 130 g (58% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126998B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-be093959ea8b46099be8a39c8ed20bf7 |
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| Source note | uspto-grants-2015_09 |
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