HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523549Generated: October 26, 2026
Chloroiodomethane → (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone
https://huagongshe.com/reaction/1523549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroiodomethane | HCID 11644 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate | HCID 853165 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone | HCID 86644148 | 42% |
Reaction Steps
To a solution of (S)-methyl 2,2-dimethyl-1,3-dioxolane-4-carboxylate (1.3 g, 8.1 mmol) and chloroiodomethane (4.3 g, 24 mmol) in THF (50 mL) at −78° C. was added a solution of LDA (16.2 mL, 24 mmol) in portions over 10 minutes. The reaction was stirred at −78° C. for 10 minutes. To this mixture was added a 10% solution of acetic acid (50 mL) in THF at −78° C. After addition, the slurry was warmed to ambient temperature. The reaction was poured into EtOAc (200 mL) and the aqueous layer basified using 1N NaOH. The organics were separated and washed with brine, dried over MgSO4 and concentrated in vacuo. The material was purified by chromatography using DCM as eluent to give (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone (0.60 g, 3.4 mmol, 42% yield) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079890B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-31947033ea6a43b1869f04a67173fcd1 |
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| Source note | uspto-grants-2015_07 |
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