HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722518Generated: November 2, 2026
Hydrochloric Acid → Methyl 2-(2-chlorobenzylaminooxymethyl)-2-methylpropanoate
https://huagongshe.com/reaction/1722518
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 2-(2-chlorobenzylideneaminooxymethyl)-2-methylpropanoate | HCID 54572932 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 2-(2-chlorobenzylaminooxymethyl)-2-methylpropanoate | HCID 20029228 | 28.5% |
Reaction Steps
A mixture of methyl 2-(2-chlorobenzylideneaminooxymethyl)-2-methylpropanoate (10.0 grams, 0.04 mole) and borane-pyridine complex (10.4 mL; 0.12 mole) in absolute ethanol (30 mL) was cooled in an ice bath. A solution of anhydrous 6.5N hydrogen chloride in ethanol (60 mL) was then added slowly. Upon completion of addition, the reaction mixture was stirred at ambient temperature for four hours. The reaction mixture was concentrated under reduced pressure, and methylene chloride (50 mL) was added to the residue. Aqueous sodium carbonate was then added to adjust the pH to 6-7. The layers were separated, and the organic layer was dried (magnesium sulfate) and concentrated under reduced pressure to yield a mixture of a white solid and liquid. The liquid was decanted off and purified by chromatography through silica gel, eluting successively with hexane and 20:1 hexane:ethyl acetate. Appropriate fractions were combined and concentrated at reduced pressure to yield 3.1 grams of methyl 2-(2-chlorobenzylaminooxymethyl)-2-methylpropanoate as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04855480 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-c20c420274864f7495627179251c996a |
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| Source note | uspto-grants-1989_08 |
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