Diisobutylaluminum hydride → 1,4,7-Trioxaspiro[4.4]nonan-8-ol

A solution of 1,4,7-trioxaspiro[4.4]nonan-8-one (prepared from tetronic acid and ethylene glycol) (3.81 g, 26.5 mmol) in dichloromethane (20 mL) at -78° C. was treated with 32 mL of 1.0 M DIBAL in dichloromethane (32.0 mmol). The mixture was stirred one hour, quenched at -78° C. with water (12 mL total) and stirred at 25° C. until complete decomposition of the aluminum complex (two hours). The granular precipitate of alumina was filtered off, and the product was purified by flash chromatography (ether) to give Compound 7 (3.32 g, 84 percent) as a low melting solid; Rf =0.16 (Et2O); IR (thin film) νmax 3446 (bs), 1720 (w) cm-1 ; 1H NMR (500 MHz, CDCl3) δ 5.51 (bd, J =4.7 Hz, 1 H, OCHOH), 3.96-3.73 (m, 7 H, CH2 --O, OCH2CH2O, OH), 2.27 (dd, J =5.4, 13.7 Hz, 1 H, CHH), 2.05 (dd, J = 1.8, 13.7 Hz, 1 H, CHH); 13C NMR (125 MHz, CDCl3) δ 114.8, 98.2, 72.5, 64.8, 64.7, 43.1; FAB HRMS (NBA/NaI) m/e 169.0477, M+NA+ calcd for C6H10O4 169.0477.

1. customquenched at -78° C. with water (12 mL total)
2. stirringstirred at 25° C. until complete decomposition of the aluminum complex (two hours)
3. filtrationThe granular precipitate of alumina was filtered off
4. customthe product was purified by flash chromatography (ether)

ORD record

ord-5cac4c45001a4702a160da52bddf6dd2

Source dataset

uspto-grants-1993_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05264586