Poly(propylene glycol) [α-hydro-ω-hydroxypoly(oxypropylene)] of number-average molar mass Mn ≈ 2000 g · mol−1 (PPG2000) was cyclised with high conversion (ca. 75%) by reaction with dichloromethane in the presence of powdered KOH. The cyclic product was separated from chain extended polymer by preparative GPC, giving an overall yield of polymer (Mn ≈ 2000 g · mol−1, narrow molar mass distribution) in excess of 50%. Characterisation by analytical GPC and 13C NMR spectroscopy confirmed cyclisation. DEPT and 1H-coupled NMR spectra were used to show that the links in cyclic poly(oxypropylene) were 77% single acetal, 12% double acetal and 11% triple acetal (or higher). This complexity probably results from competitive reaction with water introduced with KOH.