Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348247Generated: October 27, 2026

Sodium Carbonate → (3R)-3-(triethylsilyloxy)-4-methyl-5-(2-methylthiazol-4-yl)-pent-4-enal

https://huagongshe.com/reaction/348247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium SulfiteHCID 24437—
ReactantMethyl morpholine oxideHCID 82029—
Reactant(4R)-4-(triethylsilyloxy)-5-methyl-6-(2-methylthiazol-4-yl)-1,5-hexadieneHCID 69507819—
ReactantHCID 178418268HCID 178418268—
CatalystOsmium TetroxideHCID 30318—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product(3R)-3-(triethylsilyloxy)-4-methyl-5-(2-methylthiazol-4-yl)-pent-4-enalHCID 86586609—

Reaction Steps

Osmium tetraoxide (1 wt % in THF, 20.3 mL) is added to a mixture of (4R)-4-(triethylsilyloxy)-5-methyl-6-(2-methylthiazol-4-yl)-1,5-hexadiene (13.5 g), H2O (21 mL), and N-methylmorpholine N-oxide (50% in THF, 10 mL, 0.048 mol) in tert-butanol (155 mL) at 0° C. After the resulting mixture is stirred for 12 hours, Na2SO3 (10 g) and water (5 mL) are added. The resulting solution is stirred at 25° C. for 30 minutes and then extracted with ether. The combined extracts are washed with brine, dried (Na2SO4), filtered, and concentrated. Purification by flash chromatography on SiO2 provides a 1:1 diastereomeric mixture of the diol as a colorless, viscous oil. Lead tetraacetate (19.1 g) is added portionwise over 5 minutes to a suspension of the diol (18.0 g) and Na2CO3 (8.67 g) in 500 mL of benzene at 0° C. After stirring for 15 minutes, the mixture is filtered through a SiO2 pad to afford the aldehyde product. The product is directly subjected to the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176235B2
Source datasetuspto-grants-2007_02
ORD IDord-0b0ad460ee4c4e698f70e2b0c81a848f
Source noteuspto-grants-2007_02