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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58351Generated: October 26, 2026

Triethylamine → Hex-5-EN-1-YL 2-bromo-2-methylpropanoate

https://huagongshe.com/reaction/58351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Hexen-1-olHCID 69963—
Reactant2-Bromo-2-methylpropionyl bromideHCID 88685—
SolventTetrahydrofuranHCID 8028—
ProductHex-5-EN-1-YL 2-bromo-2-methylpropanoateHCID 2082961270%

Reaction Conditions

Temperature4 °C

Reaction Steps

5-Hexen-1-ol (42.6 g), triethylamine (45.8 g), and tetrahydrofuran (0.8 L) were mixed. After ice cooling, 2-bromoisobutyryl bromide (100 g) was dropped. The reaction liquid was stirred at 4° C. for 3 hours, and then at room temperature for 15 hours. The reaction liquid was then filtered, concentrated with an evaporator, and dissolved in diethyl ether (300 mL). The solution was washed with a 1N hydrochloric acid solution (2×300 mL), a saturated sodium bicarbonate solution (2×300 mL), and distilled water (2×300 mL), in this order. After that, the organic layer was dried over sodium sulfate, filtered, and concentrated with an evaporator. The product was then purified through a silica gel column (developing solvent: hexane/ethyl acetate=15/1), and concentrated to give 74.2 g of 5-hexenyl 2-bromo-2-methylpropanate of the following chemical formula (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434794B2
Source datasetuspto-grants-2016_09
ORD IDord-b22f08d90f174701a059f2bb7641776a
Source noteuspto-grants-2016_09