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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060954Generated: October 26, 2026

Methanol → Adamantan-1-yl-dichloro-acetic acid methyl ester

https://huagongshe.com/reaction/2060954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
Reactant1-BromoadamantaneHCID 79106—
ReactantHCID 11435856HCID 11435856—
CatalystZincchlorideHCID 3007855—
SolventWaterHCID 962—
SolventHeptaneHCID 8900—
ProductAdamantan-1-yl-dichloro-acetic acid methyl esterHCID 10401264—

Reaction Steps

A 1 liter flask equipped with an argon inlet was charged with crude (2,2-dichloro-1-methoxy-vinyloxy)-trimethylsilane (129.1 g, approximately 0.389 mol) and anhydrous dichloromethane (100 ml). To the resulting solution was added 1-bromoadamantane (75.2 g, 0.349 mol) and anhydrous zinc chloride (6.56 g, 48 mmol). The resulting mixture was allowed to stir at room temperature overnight. The resulting red-brown mixture was diluted with heptane (600 ml) and water (300 ml). The organic layer was separated and washed with water (2×100 ml), 1 N sodium bicarbonate (3×150 ml), and water (2×200 ml). The resulting solution was filtered though a pad of Celite 545 and filtrate was concentrated at reduced pressure to give a colorless solid. This material was dissolved in boiling methanol (250 ml). The resulting solution was allowed to cool to room temperature for 1 hour. After cooling to approximately 5° C. for 2 hours, the solid was collected by filtration and washed with cold methanol:water (94:6; 4×50 ml) to give adamantan-1-yl-dichloro-acetic acid methyl ester (Formula VII) as a colorless solid: 75.0 grams (77.3% based on 1-bromoadamantane); mp 76.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278462B2
Source datasetuspto-grants-2012_10
ORD IDord-31a1f5551ba34d379a35f4d31074ab36
Source noteuspto-grants-2012_10