HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80378Generated: October 28, 2026
Triethylamine → HCID 22476037, compound
https://huagongshe.com/reaction/80378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphine | HCID 24404 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | N-(Tetrahydro-2H-pyran-4-yl)glycine | HCID 21223365 | — |
| Reactant | Hydrate;hydrochloride | HCID 21885828 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22476037 | HCID 22476037 | 43% |
Reaction Steps
2-(tetrahydro-2H-pyran-4-ylamino)acetic acid (0.2 g, 1.256 mmol) F44 was dissolved in DMF (22.5 mL) and Et3N (2.5 mL, 17.94 mmol). After 5 minutes BOC2O (0.583 mL, 2.51 mmol) was added and the reaction solution was heated to 60° C. for 1 h. The reaction was concentrated by reduced pressure providing a light yellow oil to which was added 20 mL HCl/H2O which was adjusted to PH3 at 0° C. and stirred for 10 minutes. The reaction mixture was extracted by ethyl acetate 3×20 mL, dried (MgSO4), filtered, and concentrated to dryness. Ether was added and the mixture was sonicated and filtered providing a white solid F45 2-(tert-butoxycarbonyl(tetrahydro-2H-pyran-4-yl)amino)acetic acid (0.14 g, 0.540 mmol, 43.0% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846023B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-836c9694f43e4610ada1ad9849df3abd |
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| Source note | uspto-grants-2014_09 |
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