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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267852Generated: October 25, 2026

1,3-Dimethyladamantane → 1-Ethyladamantane

https://huagongshe.com/reaction/267852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DimethyladamantaneHCID 12800—
ReactantAcenaphthylene, dodecahydro-HCID 102215—
Product1-EthyladamantaneHCID 522637—

Reaction Steps

The same experiment as described in 2th line from the bottom in Table 5 of Example 5 was carried out except that perhydroacenaphthene prepared by hydrogenation of acenaphthene was used in place of TMN. Conversion rate of perhydroacenaphthene was 75.4%, and 1,3-dimethyladamantane and 1-ethyladamantane were obtained at 33.0% and 47.1% of selectivity and at 24.9% and 35.0% of yield respectively. Moreover, when amounts of catalyst was increased from 2 g to 4 g, conversion rate of perhydroacenaphthene was 85.6%, and 1,3-dimethyladamantane and 1-ethyladamantane were obtained at 45.2% and 6.6% of selectivity and at 38.7% and 5.7% of yield respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03944626
Source datasetuspto-grants-1976_03
ORD IDord-e1089c161b5944de91ab0aea965c0111
Source noteuspto-grants-1976_03