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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280816Generated: November 1, 2026

Acetic Acid → HCID 12015899, compound

https://huagongshe.com/reaction/1280816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTrimethylsilyl isocyanateHCID 70696—
ReactantHCID 6183558HCID 6183558—
Reactanttert-butyl 2-(1-benzyl-2-ethyl-1H-indol-4-yloxy)acetateHCID 12015898—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12015899HCID 1201589969%

Reaction Steps

A solution of 2.3 g (6.3 mmol) [[2-ethyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]acetic acid tert-butyl ester and 4.8 g (12.6 mmol) bis(2,2,2-trichloroethyl)azodicarboxylate in diethyl ether was stirred for 24 hours at room temperature. The resulting solid was filtered and vacuum dried. This adduct (1 g, 1.3 mmol) was dissolved in 10 mL of THF and treated with zinc (1 g) and glacial acetic acid (0.5 mL). After stirring for 30 minutes at room temperature an excess of trimethylsilylisocyanate in 1 mL of THF was added stirring was continued at room temperature for 18 hours. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4 and concentrated to dryness to give 0.385 g (69% yield) of the subtitled material. Mass spectrum: 423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451839B1
Source datasetuspto-grants-2002_09
ORD IDord-872616fdf8624e3cb302ec74d38e75b9
Source noteuspto-grants-2002_09