Diethylene Glycol → Hydroxy-PEG2-CH2CO2t-Bu

A solution of 53 g of 2-hydroxyethyl ether (0.5 mol) in 200 mL of tetrahydrofuran was prepared, and the solution cooled in an ice-water bath. The solution was placed under a slow stream of argon. Sodium bis(trimethylsilyl)amide (125 mL, 0.125 mol, 1 M in tetrahydrofuran) was added dropwise over a 30 minute period. The mixture was stirred an additional 30 minutes, then 24.4 g of tert-butyl 2-bromoacetate (0.125 mol) was added. The mixture was then stirred for 1 hour. The ice-water bath was removed, and the mixture transferred to a separatory funnel using 250 mL of 1 M NaH2PO4. The mixture was extracted with ethyl acetate (3×150 mL). The combined extracts were dried over sodium sulfate, filtered, and the solvent removed by rotary evaporator to give a clear yellow liquid. The liquid was purified by chromatography using 500 mL of silica gel and eluting with ethyl acetate/hexanes 1:1. The product was isolated as a clear, gold liquid. Obtained 5.49 g TLC Rf 0.50 (EtOAc). NMR (DMSO-d6)δ 1.42 (s, 9H), 3.42 and 3.54 (m, 8H), 3.98 (s, 2H).

1. temperaturethe solution cooled in an ice-water bath
2. stirringThe mixture was then stirred for 1 hour
3. customThe ice-water bath was removed
4. customthe mixture transferred to a separatory funnel
5. extractionThe mixture was extracted with ethyl acetate (3×150 mL)
6. dry with materialThe combined extracts were dried over sodium sulfate
7. filtrationfiltered
8. customthe solvent removed by rotary evaporator
9. customto give a clear yellow liquid
10. customThe liquid was purified by chromatography
11. washeluting with ethyl acetate/hexanes 1:1
12. customThe product was isolated as a clear, gold liquid

ORD record

ord-3571b92933f64b06bc90ecbe70419f5a

Source dataset

uspto-grants-1992_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05162505