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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174323Generated: November 2, 2026

Hexane → HCID 17932014, compound

https://huagongshe.com/reaction/2174323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDimethylacetamideHCID 31374—
ReactantTert-butyl 2,2,2-trichloroethanimidateHCID 2734700—
ReactantHCID 21197492HCID 21197492—
CatalystBoron trifluoride etherateHCID 8000—
SolventChloroformHCID 6212—
SolventCyclohexaneHCID 8078—
ProductHCID 17932014HCID 1793201479.1%

Reaction Steps

To a solution of α-bromoglutaric acid-5-benzylester (See Example 18a(i)(a); 1.2 g, 4.0 mmol) in chloroform (Merck, 5 mL) a solution of tert-butyl 2,2,2-trichloroacetimidate (Fluka, 1.57 mL, 8.52 mmol) in cyclohexane (Merck, 5 mL) was added dropwise over 5 minutes. N,N-Dimethylacetamide (Fluka, 0.88 mL) was added followed by boron trifluoride ethyl etherate (Aldrich, 80 μL) as catalyst. The reaction mixture was stirred for 5 days at room temperature. Hexane was added and the organic phase washed with brine three times, dried over sodium sulphate and evaporated under reduced pressure. The crude product was purified using normal phase chromatography (Silica column (40 g), solvents: A=hexane, B=ethyl acetate, gradient: 10 to 35% B over 15 min, flow rate 40 mL/min, UV detection at 214 and 254 nm) affording 1.13 g (79%) of the pure product. Structure was verified by NMR

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061080B2
Source datasetuspto-grants-2015_06
ORD IDord-05082266f0714dfaa634dbb968f0fe93
Source noteuspto-grants-2015_06