HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20009Generated: October 24, 2026
Tetrahydrofuran → 1-(2,2-Dimethoxyethyl)cyclopropan-1-ol
https://huagongshe.com/en/reaction/20009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl 3,3-dimethoxypropionate | HCID 81924 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(2,2-Dimethoxyethyl)cyclopropan-1-ol | HCID 59417281 | — |
Reaction Steps
To a 1.0 L RBF containing methyl 3,3-dimethoxypropanoate (17.6500 g, 119 mmol) was added THF (150 ml) and diethyl ether (150 ml), and the mixture was allowed to stir at 0° C. for 15 min. At this time, tetra-isopropoxy titanium (6.98 ml, 23.8 mmol) was added in one portion before the dropwise addition of ethylmagnesium bromide (99.3 ml, 298 mmol) via syringe. The reaction was allowed to warm to 23° C. and stir for 14 hours before being re-chilled to 0° C. After 5 min at this temp, water (15 ml) was added and a solid formed. Diethyl ether (200 ml) was added and the quenched reaction was stirred for 10 min before filtering through a plug of magnesium sulfate. The filtrate was dried with additional magnesium sulfate, filtered and concentrated to give a colorless oil. The crude material was used directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745484B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-6fee97b78a4a47b3b51493577f890479 |
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| Source note | uspto-grants-2010_06 |
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