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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30408Generated: October 29, 2026

Diethyl Ether → HCID 57420555, compound

https://huagongshe.com/reaction/30408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 3-(hydroxymethyl)-3-methylpiperidine-1-carboxylateHCID 22258928—
SolventDichloromethaneHCID 6344—
ProductHCID 57420555HCID 5742055597.9%

Reaction Steps

To a 0° C. stirred solution of Intermediate 55 (0.844 g, 3.68 mmol) in dry CH2Cl2 (25 ml) was added Et3N (0.513 ml, 3.682 mmol) and the reaction was stirred for 15 minutes. Methansulfonyl chloride (0.285 ml, 3.682 mmol) was added dropwise and the reaction was allowed to warm to room temperature overnight with good stirring. The reaction was complete by TLC, and Et2O (100 ml) was added. The mixture was filtered and the filter caked was washed with additional Et2O. The filtrate was then concentrated under reduced pressure. The residue was chromatographed with hexanes/EtOAc (0>25%) to yield 1.05 g (93.1%) of 3-methanesulfonylmethyl-3-methyl-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 56). 1H NMR (400 MHz, CDCl3) δ ppm 1.0 (s, 3 H), 1.4 (m, 1 H), 1.4 (s, 9 H), 1.6 (m, 3 H), 3.0 (s, 3 H), 3.2 (s, 1 H), 3.5 (s, 2 H), 4.0 (d, J=2.4 Hz, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423054B2
Source datasetuspto-grants-2008_09
ORD IDord-786aff377e384a54b03121697a243557
Source noteuspto-grants-2008_09