HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552257Generated: October 31, 2026
Acetic Acid → 4-(1,4-Dioxaspiro[4.5]decan-8-yl)morpholine
https://huagongshe.com/reaction/552257
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(1,4-Dioxaspiro[4.5]decan-8-yl)morpholine | HCID 53486356 | 81.7% |
Reaction Steps
Sodium triacetoxyborohydride (382 g, 1.8 mol) was added in one portion to a mixture of 1,4-dioxaspiro[4.5]decan-8-one (200.0 g, 1.28 mol), morpholine (111.4 g, 1.28 mol) and glacial AcOH (73.2 mL, 1.28 mol) in 1,2-dichloroethane (4 L). A slightly exothermic reaction occurred accompanied by increase in temperature by 12° C. Then the mixture was stirred at room temperature overnight. The reaction was quenched by the addition of 10% aqueous NaOH (1.8 L) over a period of 20 min. The organic layer was separated, washed with brine (1 L), dried over MgSO4 and concentrated to afford 1 (237.66 g) as white solid. The aqueous layer was extracted with AcOEt (4×300 mL). Combined extracts were washed with brine (1 L), dried over MgSO4 and concentrated to furnish additional portion of 1 (44 g) as an off-white solid. Total yield of 1 (281.66 g, 97%). 1H NMR data identical with the data obtained earlier.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951802B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-8e3d0e0d39d74219afc31d014d929051 |
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| Source note | uspto-grants-2011_05 |
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