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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499330Generated: November 1, 2026

Triethylamine → HCID 87578542, compound

https://huagongshe.com/reaction/1499330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-2-methylpropionyl bromideHCID 88685—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 57912296HCID 57912296—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87578542HCID 8757854260%

Reaction Steps

TBAF (4.19 mL of a 1.0 M solution in THF) was added dropwise to a stirring solution of Compound 11 (487 mg, 1.40 mmol) in THF (14 mL). TLC analysis showed complete reaction after 5 minutes, after which time the THF was removed on a rotary evaporator and the resulting oil was dissolved in EtOAC (50 mL), washed with saturated NH4Cl (2×20 mL), water (2×50 mL), dried over MgSO4, concentrated in vacuo. The resulting white solid (Compound 12) was dissolved in anhydrous THF (14 mL), triethylamine (184 mg, 1.81 mmol) was added, and the resulting solution was added dropwise to a stirring solution of □-bromoisobutyrylbromide (225 mg, 1.82 mmol) in THF (5 mL) at 0° C., A white precipitate formed immediately. The mixture was allowed to warm to room temperature and stirred overnight under argon atmosphere after which time the solid salts were filtered, and the solvent was removed on a rotary evaporator. The resulting yellow oil was dissolved in ethyl acetate (50 mL) and washed with water (3×20 mL), dried over MgSO4, concentrated in vacuo, and purified by silica gel chromatography (50% EtOAc:hexane) to yield Compound 13 (321 rag, 60%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200097B2
Source datasetuspto-grants-2015_12
ORD IDord-b7a242a4daa64d6ea1d2368f4297f70b
Source noteuspto-grants-2015_12