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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508392Generated: November 1, 2026

Trimethyl orthoacetate → HCID 68505210, compound

https://huagongshe.com/reaction/1508392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoacetateHCID 15050—
ReactantHCID 86608775HCID 86608775—
Catalystp-Toluenesulfonic acidHCID 6101—
ProductHCID 68505210HCID 6850521072.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Tert-butyl 3-(2-(3-(tert-butyldimethylsilyloxy)phenyl)-5-(2,5-difluorophenyl)-3-(hydrazinecarbonothioyl)-2,3-dihydro-1,3,4-thiadiazol-2-yl)propylcarbamate (100 mg, 0.157 mmol) was weighed into a 25 mL flask and suspended in 5.0 mL of 1,1,1-trimethoxyethane (5 mL, 0.157 mmol). 4-methylbenzenesulfonic acid (0.540 mg, 0.00314 mmol) was then added, and the reaction heated to 80° C. for 1 hour. The reaction mixture was concentrated in vacuo, and the residue was purified by flash column chromatography (20-50% ethyl acetate/hexanes), to afford 75 mg (72% yield) of the desired product as a yellow solid on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221841B2
Source datasetuspto-grants-2015_12
ORD IDord-faef69d3a64b4acb88bebe60a0cd2462
Source noteuspto-grants-2015_12