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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304632Generated: November 1, 2026

Acetic Acid → HCID 12015899, compound

https://huagongshe.com/reaction/2304632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTrimethylsilyl isocyanateHCID 70696—
ReactantBis(2,2,2-trichloroethyl) AzodicarboxylateHCID 4678091—
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 is stirred for 24 hours at room temperature. The resulting solid is filtered and vacuum dried. This adduct (1 g, 1.3 mmol) is 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 trimethyisiiyiisocyanate in 1 mL, of THF is added and stirring is continued at room temperature for 18 hours. The mixture is diluted with water and extracted with ethyl acetate. The organic layer is 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 numberUS06436983B1
Source datasetuspto-grants-2002_08
ORD IDord-b91f25028a20462089708c4cb9447e51
Source noteuspto-grants-2002_08