HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283006Generated: October 30, 2026
Sodium Hydroxide → 2-Hydroxymethyl-4-n-propylmorpholine
https://huagongshe.com/reaction/1283006
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Allyloxymethyl-4-n-propylmorpholine | HCID 21430412 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxymethyl-4-n-propylmorpholine | HCID 21430425 | 35% |
Reaction Steps
2-Allyloxymethyl-4-n-propylmorpholine (59.7 g.) is heated under reflux in hydrochloric acid (240 ml., 20%) for 18 hours. The solution is cooled, diluted with ice and water, and basified with sodium hydroxide and extracted with ether (3 × 200 ml.). The ethereal solution is dried (MgSO4) filtered and the ether evaporated to give recovered starting material. The aqueous layer is concentrated to a small volume and precipitated salt is removed by filtration and washed with ether. The filtrate is extracted with ether (3 × 100 ml.) and the combined extracts and ethereal wash are dried (MgSO4) filtered and the ether evaporated. 2-Hydroxymethyl-4-n-propylmorpholine (16.7 g.) is obtained as a viscous oil which forms a hydrogen oxalate, m.p. 133°-135°C. after crystallisation from a methanol/ether mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03974156 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-1f0368abc55048e3a9dfc80ef4ba744c |
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| Source note | uspto-grants-1976_08 |
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