Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644293Generated: October 29, 2026

Chloromethyl Methyl Ether → Methyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-(methoxymethoxy)benzoate

https://huagongshe.com/reaction/644293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-hydroxybenzoateHCID 68532897—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-(methoxymethoxy)benzoateHCID 6853550996.4%

Reaction Steps

Methyl 2-(1-tert-butoxycarbonylpiperidin-4-yloxy)-4-hydroxybenzoate (9.13 g, 26.0 mmol) was dissolved in DMF. Potassium carbonate (7.19 g, 52.0 mmol) was added, followed by methoxymethyl chloride (2.51 g, 31.2 mmol), and the reaction was stirred at room temperature under a drying tube for 24 h. An additional 1.2 eq of methoxymethyl chloride was added and the reaction stirred an additional 48 h. The DMF was removed in vacuo. The residue was dissolved in ethyl acetate, washed with water, dried, and the solvent was removed in vacuo to give 9.91 g (96.2%) of a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700628B2
Source datasetuspto-grants-2010_04
ORD IDord-88a01cbd42274191ab02e8fa7a136112
Source noteuspto-grants-2010_04