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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185566Generated: November 1, 2026

Pivaloyl chloride → HCID 22458230, compound

https://huagongshe.com/reaction/2185566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)propanoic acidHCID 1512540—
SolventDichloromethaneHCID 6344—
ProductHCID 22458230HCID 2245823050%

Reaction Steps

A solution of 3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propionic acid (2.6 grams, 10 mmol, from Step A) and DIEA (4.4 mL, 25 mmol) in 50 mL CH2Cl2 was cooled to 0° C. Trimethylacetyl chloride (1.4 mL, 11 mmol) was added and the mixture was stirred for 1 h. Solid N,O-dimethylhydroxylamine hydrochloride (1.4 grams, 15 mmol) was added and the mixture was warmed to rt and stirred for 16 h. The solvent was removed and the product was purified by flash chromatography (125 grams silica, 2/1 hexane/EtOAc eluant) to give 1.5 grams (50%) of the title compound. 1H NMR (300 MHz, CDCl3). δ1.05-1.18 (m, 2H), 1.45 (s, 9H), 1.53-1.75 (m, 4H), 2.4-2.5 (t, 2H), 2.6-2.77 (m, 2H), 3.18 (s, 3H), 3.63 (s, 3H), 4.0-4.15 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399619B1
Source datasetuspto-grants-2002_06
ORD IDord-62c766c938724db0a14c145c8b5b7374
Source noteuspto-grants-2002_06