The synthesis and olfactory properties of as eries of 2-substituteda nd 2,3-annulated1 ,4-dioxepan-6-onesisr eported. By Williamson etherification with 3-chloro-2-(chloromethyl)prop-1-ene( 6)a nd subsequentK atsuki-Sharpless oxidation, 1,4-dioxepan-6-one (8a)a nd its 2-methyl (8b), 2-propyl (8c), 2-isobutyl (8d), and 2,2,3,3-tetramethyld erivative (8e), as well as four 2,3-annulated 1,4-dioxepan-6-ones 8h, 8i, 8j,a nd 8k were synthesised.B ye therification with ethyl diazoacetate and subsequent Dieckmann cyclisation, (5aS,9aS)-9-bromoand 9-iodo-5a,6,7,9a-tetrahydro-2 Hbenzo[b][1,4]dioxepin-3(4 H)-one(8f/g)aswell as a2,3-annulated derivative 8m from (+ +)-limonene were prepared. 2-Propyl-1,4-dioxepan-6-one (8c)w as discovered to have ag reen floral odourw ith anisic and cinnamic nuances, which could be rationalised by as uperpositiona nalysis. The olfactoryp roperties of the 1,4-dioxepan-6-oness ynthesised underline the crucial importance of ab enzenoid ring system for marine odorants.