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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807342Generated: October 29, 2026

Undecane → HCID 66974041, compound

https://huagongshe.com/reaction/1807342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUndecaneHCID 14257—
ReactantRed-AlHCID 16684438—
ReactantHCID 66974036HCID 66974036—
SolventTolueneHCID 1140—
ProductHCID 66974041HCID 66974041100%

Reaction Conditions

Temperature75 °C

Reaction Steps

Preparation of 2,4,8-Trimethyl-5-oxa-tricyclo[6.2.1.0*2,6]undecane (Structure 4): 4-Allyl-1,4-dimethyl-bicyclo[3.2.1]octan-3-one (288 g, 1.5 mol, obtained as above in EXAMPLE IV) was added to a solution of Red-Al (65%, 506 g, 1.5 mol) in toluene at 75° C. The reaction mixture was aged for 3 hours while the temperature was maintained at 75° C., then cooled to room temperature, and subsequently quenched with a solution of sodium bicarbonate (NaHCO3). Distillation of the organic layer provided 4-allyl-1,4-dimethyl-bicyclo[3.2.1]octan-3-ol (288 g, 1.5 mol), which was then added to a MSA solution (30 g) in toluene (500 mL) and heated to reflux for 3 hours. The reaction mixture was subsequently washed with a Na2CO3 solution. Fractional distillation of the organic layer provided 2,4,8-trimethyl-5-oxa-tricyclo[6.2.1.0*2,6*]undecane (170 g) having a boiling point of 62° C. at a pressure of 0.3 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357358B2
Source datasetuspto-grants-2013_01
ORD IDord-fa5560a3480843a5890d2fc0df1c01a4
Source noteuspto-grants-2013_01