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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990793Generated: October 26, 2026

1-Bromo-3,5-dimethyladamantane → 3,5-dimethyl-1-adamantyl Acetate

https://huagongshe.com/reaction/990793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3,5-dimethyladamantaneHCID 98317—
ReactantPotassium AcetateHCID 517044—
SolventAcetic AcidHCID 176—
Product3,5-dimethyl-1-adamantyl AcetateHCID 22633608—

Reaction Steps

2.486 (10.2 mmoles) of 3,5-dimethyl-1-bromoadamantane is refluxed for 16 hours with 2.034 g (20.7 mmoles) of potassium acetate in 10 mL of acetic acid. The solution is poured over 100 grams of ice, allowed to melt, and extracted with 3×10 mL of diethyl ether. The combined ether extracts are washed with saturated aqueous sodium bicarbonate followed by saturated aqueous sodium chloride, then dried over sodium sulfate. The solvent is removed under vacuum, yielding 1.521 (67%) of the desired product, a colorless oil. TLC: Rf=0.68 (silica plate: eluant hexane 90%, ethyl acetate 10%). 1HNMR (CDCl3, 500 Mhz): 0.858 (s, 6H), 1.115 (d, 2H, J=12.4 Hz), 1.177 (d, 2H, J=12.4 Hz), 1.260 (d, 2H, J=12.3 Hz), 1.367 (d, 2H, J=12.3 Hz), 1.714 (d, 2H, J=11.6 Hz), 1.766 (d, 2H, J=11.6 Hz), 1.939 (s, 2H), 1.976 (s, 3H), 2.191 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462064B1
Source datasetuspto-grants-2002_10
ORD IDord-c5fff817438c4d5c9d427af5bcaa9e31
Source noteuspto-grants-2002_10