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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853045Generated: October 28, 2026

Sodium hydride → HCID 69414220, compound

https://huagongshe.com/reaction/853045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(s)-Tert-butyl 5-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxideHCID 11195739—
ReactantEthyl 6-(trifluoromethyl)-1H-indole-2-carboxylateHCID 22311001—
SolventDimethylformamideHCID 6228—
ProductHCID 69414220HCID 6941422088%

Reaction Conditions

Temperature5 °C

Reaction Steps

Sodium hydride (0.75 g, 17 mmol) was suspended in N,N-dimethylformamide (15 mL) and a solution of 6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl ester (3.6 g, 14 mmol) in N,N-dimethylformamide (15 mL) was added with cooling at 5° C. After 1 h (S)-5-methyl-2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester (4.0 g, 17 mmol) was added and the solution was allowed to reach room temperature over the weekend. The solution was partitioned between ice water (600 mL) and diethylether (2-×250 mL). The organic layer was washed with ice water and brine, dried (MgSO4), and evaporated. Chromatography on silica gel with n-hexane/diethylether (4:1) yielded the title product as yellow oil (5.1 g, 88%). ISP-MS: m/e=415.3 (M+H+), αD20=−29.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253281B2
Source datasetuspto-grants-2007_08
ORD IDord-8ec37c4ca20e4a04ba5696ac3869d3b3
Source noteuspto-grants-2007_08