HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554850Generated: October 26, 2026
Water → 2-Chloro-3-oxo-pentanedioic acid diethyl ester
https://huagongshe.com/reaction/554850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Diethyl acetonedicarboxylate | HCID 66045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-3-oxo-pentanedioic acid diethyl ester | HCID 86640001 | 215.2% |
Reaction Steps
Dissolve 3-oxo-pentanedioic acid diethyl ester (1122 g, 5.327 mol) in CH2Cl2 (3 L) and cool to −9° C. To the above solution, slowly add a solution of sulfuryl chloride (374 g, 2.69 mol) in CH2Cl2 (3 L) over 3 h. Upon completion, add a second charge of sulfuryl chloride (374 g, 2.69 mol) in CH2Cl2 (3 L) over 4 h. Stir the resulting cooled solution for one hour, then warm to room temperature and stir overnight. Cool the solution in an ice bath and slowly add water (8 L). Stir for 15 min, then separate the layers. Extract the aqueous layer with additional CH2Cl2. Combine the organic phases and wash with saturated NaHCO3 (3 L). Dry and concentrate the organic solution to obtain 1370 g (105%) of the title compound as a colorless oil. Use the material as-is in the next reaction without further purification. ES/MS m/z (35Cl) 235 [M−1]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08049013B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-d7d211d82ec94155ac7da3a8bf375dd6 |
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| Source note | uspto-grants-2011_11 |
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