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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748173Generated: October 31, 2026

(((2-Methylenecyclohexyl)methoxy)methyl)benzene → 4-((Benzyloxy)methyl)spiro[2.5]octane

https://huagongshe.com/reaction/1748173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(((2-Methylenecyclohexyl)methoxy)methyl)benzeneHCID 10703955—
ReactantEthyl spiro[2.5]octane-6-carboxylateHCID 67984131—
Product4-((Benzyloxy)methyl)spiro[2.5]octaneHCID 67983984—

Reaction Steps

This intermediate was prepared from (((2-methylenecyclohexyl)methoxy)methyl)benzene by using the same protocol as described for ethyl spiro[2.5]octane-6-carboxylate (I-7A). 1H NMR (400 MHz, CDCl3) δ 7.35-7.31 (m, 4H), 7.29 (m, 1H) 4.49 (q, J=12.4 Hz, 2H), 3.52 (t, J=9.2 Hz, 1H), 3.41 (dd, J=9.2, 5.2 Hz, 1H), 1.72-1.67 (m, 1H), 1.49-1.43 (m, 4H), 1.33-1.26 (m, 1H), 0.88-0.85 (m, 1H), 0.37-0.31 (m, 2H), 0.19-0.14 (m, 2H). MS m/z 231.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150568B2
Source datasetuspto-grants-2015_10
ORD IDord-0427a2ad43f94267bec03a0e8b08f24c
Source noteuspto-grants-2015_10