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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626815Generated: November 2, 2026

Ethyl Acetate → tert-Butyl [2-(6-acetyl-4-chloro-2-formyl-3-methylphenoxy)ethyl]carbamate

https://huagongshe.com/reaction/626815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium periodateHCID 23667635—
Reactanttert-Butyl [2-(6-acetyl-4-chloro-3-methyl-2-vinylphenoxy)ethyl]carbamateHCID 86697511—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl [2-(6-acetyl-4-chloro-2-formyl-3-methylphenoxy)ethyl]carbamateHCID 8669751273%

Reaction Conditions

Temperature60 °C

Reaction Steps

tert-Butyl [2-(6-acetyl-4-chloro-3-methyl-2-vinylphenoxy)ethyl]carbamate (4.1 g, 12 mmol) was dissolved in tetrahydrofuran (300 mL) and 0.157 M osmium tetraoxide in water (10 mL) was added followed by a solution of sodium metaperiodate (7.4 g, 35 mmol) in water (20 mL). The reaction was stirred at 60° C. for 2 hours. Additional 0.157 M osmium tetraoxide in water (10 mL) and a solution of sodium metaperiodate (7.4 g, 35 mmol) in water (20 mL) were added and the mixture was heated at 60° C. for 2 more hours. The mixture was poured into ethyl acetate and washed with water, brine, dried over sodium sulfate, filtered and evaporated. Purification on silica gel using ethyl acetate in hexanes (0-12%) gave the desired compound (3.0 g, 73%) (note: elutes as 2 separate peaks in both normal and reversed phase chromatography). LCMS calculated for C17H22ClNO5Na (M+Na)+: m/z=378.1; found: 378.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309251B2
Source datasetuspto-grants-2016_04
ORD IDord-dd45a77876d243b49e46b9a8a2df1e17
Source noteuspto-grants-2016_04