HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080902Generated: October 29, 2026
1-Iodopropane → Ethyl 1-propylcyclobutane-1-carboxylate
https://huagongshe.com/reaction/2080902
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | Ethyl cyclobutanecarboxylate | HCID 84700 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 1-propylcyclobutane-1-carboxylate | HCID 14301362 | 48% |
Reaction Steps
Ethyl cyclobutanecarboxylate 1 (25.0 g, 0.195 mol) was added to a solution of lithium diisopropylamide (97.5 mL of a 2.0M solution in THF, 0.195 mol) in THF (200 mL) at −78° C. After 30 min the reaction solution was warmed to room temperature and transferred via cannula to a solution of 1-iodopropane (49.7 g, 0.293 mol) in DMSO (104 mL) while maintaining the temperature between 15-20° C. After stirring for an additional 30 min the precipitated salts were removed by vacuum filtration. The filtrate was concentrated in vacuo, diluted with hexane and washed with 1 N HCl, saturated aqueous NaHCO3 and brine. The organic portion was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by vacuum distillation (105-108° C., 20-30 mmHg) to give 16 g (48%) of the ester 2 as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932420B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-15761b5f99644c2b93179d2e0498786c |
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| Source note | uspto-grants-2011_04 |
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