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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537854Generated: October 26, 2026

Hexachloroethane → tert-butyl 2-(2-chlorooxazol-5-yl)-1H-indole-1-carboxylate

https://huagongshe.com/reaction/537854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-butyl 2-(oxazol-5-yl)-1H-indole-1-carboxylateHCID 71060685—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 2-(2-chlorooxazol-5-yl)-1H-indole-1-carboxylateHCID 7106019799.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

LiHMDS (1.06 M in THF, 9.54 mL, 10.00 mmol) was added to a solution of tert-butyl 2-(oxazol-5-yl)-1H-indole-1-carboxylate 20 (2.37 g, 8.34 mmol) in THF (20 mL) at −78° C., and the mixture was stirred at −78° C. for 1 h. A solution of hexachloroethane (2.96 g, 12.50 mmol) in THF (5 mL) was added at −78° C., and the mixture was stirred at −78° C. for 2 h and allowed to warm to room temperature and stirred for 14 h. The reaction was quenched by adding EtOAC: H2O (50 mL: 15 mL), and then extracted with Ethyl acetate. The extracts were washed with brine, dried (Na2SO4) and concentrated. The product was purified by column chromatography (Acetone/hexane as an eluent) to provide tert-butyl 2-(2-chlorooxazol-5-yl)-1H-indole-1-carboxylate 21 (2.64 g, 99% yield) as white solid. MS (ES) m/z 319 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865709B2
Source datasetuspto-grants-2014_10
ORD IDord-0e55799e16f0453297a1c06e2771c461
Source noteuspto-grants-2014_10