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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400784Generated: October 31, 2026

Ether hydrochloride → 4-((Allyloxy)methyl)-4-methylpiperidine

https://huagongshe.com/reaction/1400784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEther hydrochlorideHCID 10953452—
ReactantTert-butyl 4-((allyloxy)methyl)-4-methylpiperidine-1-carboxylateHCID 86710836—
Product4-((Allyloxy)methyl)-4-methylpiperidineHCID 86710837117.2%

Reaction Steps

tert-Butyl 4-((allyloxy)methyl)-4-methylpiperidine-1-carboxylate (300 mg, 1.114 mmol) was placed in a 25 mL RBF. A 2N solution of HCl/ether was added (7 mL) and the vessel was sealed with a septa. The colorless homogeneous solution was stirred for 24 h. An aliquot was removed and analyzed by 1H NMR which indicated that the reaction was complete. The reaction mixture was concentrated in vacuo to give 221 mg (96%) of 4-((allyloxy)methyl)-4-methylpiperidine as a white sticky solid. 1H NMR (500 MHz, DMSO-d6) δ 8.88-8.42 (m, 2H), 5.90 (ddt, J=17.3, 10.5, 5.2 Hz, 1H), 5.35-5.12 (m, 2H), 3.96 (dt, J=5.2, 1.5 Hz, 2H), 3.24-3.16 (m, 2H), 3.12-2.93 (m, 4H), 1.70 (ddd, J=14.3, 10.0, 4.3 Hz, 2H), 1.43 (dt, J=14.2, 4.4 Hz, 2H), 0.98 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906929B2
Source datasetuspto-grants-2014_12
ORD IDord-4d8feb5366a749798edc89c6aa6db36c
Source noteuspto-grants-2014_12