HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904526Generated: November 1, 2026
Piperidin-2-ylmethanol → HCID 20037300, compound
https://huagongshe.com/reaction/1904526
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidin-2-ylmethanol | HCID 94263 | — |
| Reactant | 4-Chloro-2-fluoro-5-methoxyphenyl isothiocyanate | HCID 11031300 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20037300 | HCID 20037300 | 98% |
Reaction Steps
11.5 g (0.10 mol) of 2-hydroxymethylpiperidine are dissolved in 100 ml of ether, and 21.8 g (0.10 mol) of 4-chloro-2-fluoro-5-methoxyphenyl isothiocyanate are added dropwise at RT. The mixture is stirred for 2 hours at 30° C., washed with twice 100 ml of water and dried over sodium sulfate, and the solvent is removed. 32.6 g (98% of theory) of 1-[N-(4-chloro-2-fluoro-5-methoxyphenyl)thiocarbamoyl]-2-hydroxymethylpiperidine are obtained in the form of a pale yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04838931 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-257b6cec90d84b01a64323d2befd5729 |
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| Source note | uspto-grants-1989_06 |
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