HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662969Generated: October 26, 2026
Dichloromethane → Dichloromethane piperidine
https://huagongshe.com/reaction/1662969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | Dichloromethane piperidine | HCID 67144590 | — |
Reaction Steps
If R1 and R2 are both hydrogen preferably the first stage is carried out as follows: the aminooxy-2-chlortrityl polystyrene resin is mixed in a suitable solvent, such like dichloromethane, with a compound of formula VI, in which R1 and R2 are both hydrogen, in the presence of 1-hydroxybenzotriazole hydrate and 1,3-diisopropylcarbodiimide and the resulting mixture then treated with N-ethyl-diisopropylamine at room temperature. The obtained resin is isolated and shaken twice for a period of 15 to 45 minutes, e.g. 20 minutes, with a freshly prepared dichloromethane/piperidine solution to provide a compound of formula VII, in which the black circular plane indicates that the compound is bound to a polymer resin and in which R1 and R2 are both hydrogen.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034810B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-b00ff416727040d5ab4da016ca7a5d04 |
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| Source note | uspto-grants-2011_10 |
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