Dimethyl Sulfoxide → (S)-3-benzyloxy-2-methylpropanal

Temperature

-78 °C

An oven dried three-necked 2 L round bottom flask was equipped with a mechanical stirrer, a thermometer, an N2 inlet, and a septum. The flask was charged with 24.050 g (0.189 mol) of oxalyl chloride and 425 mL CH2Cl2. The reaction mixture was stirred under an N2 atmosphere and cooled to −78° C. with an external dry ice-acetone bath. A solution of methyl sulfoxide (29.607 g; 0.379 mol) in 85 mL CH2Cl2 was then added over 5 min to the reaction mixture via cannula. After the adition, the reaction was stirred an additional 5 min and then a solution of 31.048 g (0.172 mol) of (S)-3-benzyloxy-2-methylpropan-1-ol in 170 mL CH2Cl2 was added via cannula. When the second addition was completed the reaction mixture was stirred for 15 min at −78° C. then 111.32 g (0.861 mol) of N,N-diisopropylethylamine was added via syringe. The reaction mixture was stirred an addition 15 min at −78° C., the cooling bath was removed and the reaction was allowed to warm. When the internal temperature had reached −15° C., 350 mL of a 10% aqueous NaHSO4 solution was slowly added and the mixture was transferred to a separatory funnel. The organic layer was separated, washed with aqueous NaHSO4 (2×250 mL), saturated NaCl, dried (MgSO4), filtered and evaporated. The residue was used immediately in the next step without further purification.

1. customAn oven dried three-necked 2 L round bottom flask was equipped with a mechanical stirrer
2. stirringAfter the adition, the reaction was stirred an additional 5 min
3. additionWhen the second addition
4. stirringwas stirred for 15 min at −78° C.
5. stirringThe reaction mixture was stirred
6. additionan addition 15 min at −78° C.
7. customthe cooling bath was removed
8. temperatureto warm
9. customhad reached −15° C.
10. addition350 mL of a 10% aqueous NaHSO4 solution was slowly added
11. customthe mixture was transferred to a separatory funnel
12. customThe organic layer was separated
13. washwashed with aqueous NaHSO4 (2×250 mL), saturated NaCl
14. dry with materialdried (MgSO4)
15. filtrationfiltered
16. customevaporated
17. customThe residue was used immediately in the next step without further purification

ORD record

ord-789e754b13414e6c9d7cc34a9fc7b0a4

Source dataset

uspto-grants-2001_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06180642B2