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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040415Generated: October 26, 2026

Hydrochloric Acid → Menthyl bromoacetate

https://huagongshe.com/reaction/2040415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMentholHCID 1254—
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
SolventTetrahydrofuranHCID 8028—
ProductMenthyl bromoacetateHCID 515297551%

Reaction Steps

To a solution of (−) Menthol (2.75 mmoles) in anhydrous THF (5 ml), Et3N (2.75 mmoles) is added under stirring. The solution temperature is lowered to 0° C. and bromo-acetylbromide (2.5 mmoles) added. The solution temperature is then allowed to raise to room temperature and the reaction mixture is stirred for 2 hours. An HCl 1N (2 ml) aqueous solution is added and the organic phase is extracted with ethyl acetate (3×5 ml). The pooled organic phases are washed with a saturated aqueous NaCl solution (1×15 ml), dehydrated on Na2SO4 and filtered. The solvent is evaporated under a reduced pressure and the crude product is purified by flash chromatography in n-hexane/ethyl acetate 97/3 volume/volume. 388 mg of 2-isopropyl-5-methyl-cyclohexyl ester of the bromo acetic acid (51% yield) are recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580820B2
Source datasetuspto-grants-2013_11
ORD IDord-253674b0829845ddbdc9e69de36d131b
Source noteuspto-grants-2013_11