HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035299Generated: October 26, 2026
(2,5-Dimethylphenyl)acetyl chloride → HCID 66794133, compound
https://huagongshe.com/reaction/2035299
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2,5-Dimethylphenyl)acetyl chloride | HCID 22561615 | — |
| Reactant | HCID 23202903 | HCID 23202903 | — |
| Reactant | 4-Hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester | HCID 59584750 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 66794133 | HCID 66794133 | — |
Reaction Steps
To a solution of 4-hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester (1.0 g, 4.92 mmol) in 10 ml pyridine under argon was added 4-dimethylaminopyridine DMAP (30 mg, 0.25 mmol). The solution was cooled down to 0° C., then (2,5-dimethyl-phenyl)-acetyl chloride (0.99 g, 5.4 mmol) was added dropwise. The reaction mixture was warmed up to room temperature and left stirring for 5 days. Then the reaction mixture was concentrated and the crude product was purified by column chromatography on silica gel (ethyl acetate/cyclohexane first 1:15, then 1:9) to give pure 4-[2-(2,5-dimethyl-phenyl)-acetoxy]-1-methoxy-piperidine-4-carboxylic acid ethyl ester (compound P3.2) as light yellow oil. Yield: 530 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08574607B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-12db9e4a17a34c36982881ee8abcb862 |
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| Source note | uspto-grants-2013_11 |
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