HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511014Generated: October 26, 2026
Chloroiodomethane → (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone
https://huagongshe.com/reaction/1511014
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 | 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. After addition, the slurry was warmed to ambient temperature. The reaction was poured into EtOAc (200 mL) and the aqueous layer basified using 1 N 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 |
|---|
| Patent number | US08212045B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-3420a5cfa3d74fae89e5a04f85a5db03 |
|---|
| Source note | uspto-grants-2012_07 |
|---|