HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473791Generated: October 30, 2026
Methanol → 4-Hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/1473791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Hydroxyamino-1-methoxy-piperidine-4-carboxylic acid | HCID 86657467 | — |
| Product | 4-Hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl ester | HCID 86657465 | — |
Reaction Steps
To a suspension of 4-hydroxyamino-1-methoxy-piperidine-4-carboxylic acid (1.0 g, 5.26 mmol) in methanol (25 ml) at 0-10° C. was added thionyl chloride (1.14 ml, 1.88 g, 15.77 mmol) and the reaction mixture was heated at reflux for 48 hours. After cooling, the mixture was concentrated, the residue diluted with ice water (20 ml) and neutralised with aqueous sodium bicarbonate. The aqueous phase was extracted with diethyl ether (3×25 ml), the combined organic layers washed with aqueous sodium bicarbonate and brine, dried over sodium sulfate and concentrated. Yield: 0.53 g of 4-hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl ester (title compound P4ii.2) as a viscous, yellowish oil. This material was identical to the compound described above under preparation ‘EXAMPLE 11, Step 3’.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018135B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-c412afc450e244a89538b18655c3584a |
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| Source note | uspto-grants-2015_04 |
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