HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951753Generated: October 25, 2026
Iodine → [8-(3-Methoxypropyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-dimethylamine
https://huagongshe.com/reaction/1951753
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Chloro-3-methoxypropane | HCID 118927 | — |
| Reactant | 8-(Dimethylamino)-1,4-dioxaspiro[4.5]decane-8-carbonitrile | HCID 360977 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [8-(3-Methoxypropyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-dimethylamine | HCID 68842849 | — |
Reaction Steps
A solution of 1-chloro-3-methoxy-propane (10.0 g, 92 mmol) in abs. ether (15 ml) was added dropwise, under an argon atmosphere and with intermittent heating, to magnesium (10.0 g, 92 mmol) and I2 in abs. diethyl ether (30 ml). Then the mixture was stirred under reflux for 60 min., following which the magnesium had not dissolved completely. While cooling with ice, a solution of 8-dimethylamino-1,4-dioxa-spiro[4.5]decane-8-carbonitrile B-1 (9.68 g, 46 mmol) in abs. THF (30 ml) was added dropwise. A viscous precipitate formed, and 100 ml of THF were then added for the purpose of better mixing. The mixture was stirred for 24 h at room temperature. 20% NH4Cl solution (100 ml) and water (120 ml) were added to the mixture, while cooling with ice, the organic phase was separated and the aqueous phase was extracted with ether (3×120 ml). The combined organic phases were washed with saturated NaCl solution (120 ml) and water (120 ml), dried over Na2SO4 and concentrated in vacuo. The crude yield was 10.8 g of brown oil. 9.8 g of crude product were purified by flash chromatography with CHCl3/MeOH (50:120:19:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404740B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-70496bff104240f6b3c7686ec9ba48e5 |
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| Source note | uspto-grants-2013_03 |
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