HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517317Generated: October 31, 2026
Hydrochloric Acid → HCID 86673312, compound
https://huagongshe.com/reaction/517317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | Ethanesulfonic acid, isopropyl ester | HCID 134677 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86673312 | HCID 86673312 | 58.3% |
Reaction Steps
A solution of ethanesulfonic acid isopropyl ester (1.0 g, 6.6 mmol) in tetrahydrofuran (15 mL) was cooled to −78° C., and n-butyllithium (1.57 M, 4.6 mL, 7.2 mmol) was added. After stirring at −78° C. for 20 minutes, diethyl chlorophosphate (0.52 mL, 3.6 mmol) was added to the reaction mixture, and the mixture was further stirred for 30 minutes. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=40/60) to give the title compound (0.61 g, 2.1 mmol, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115107B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-ac403a1030d04a33903c62970bf6762f |
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| Source note | uspto-grants-2015_08 |
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