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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605445Generated: October 25, 2026

Hydrochloric Acid → 6-(Acryloyloxy)hexanoic acid

https://huagongshe.com/reaction/605445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcryloyl chlorideHCID 13140—
Reactant6-Hydroxyhexanoic AcidHCID 14490—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDimethylacetamideHCID 31374—
Product6-(Acryloyloxy)hexanoic acidHCID 15936996—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 6-hydroxyhexanoic acid (10 g), 2,6-di-tert-butyl-4-methylphenol (0.5 g), and dimethylacetamide (57 mL) was cooled to 0° C. Acryloyl chloride (17.2 g) was then added dropwise. After stirring for 3.5 hrs, pyridine (12 mL) and water (12 mL) were slowly added. After stirring for another 2 hrs, the solution was acidified with dilute HCl and extracted with ethyl acetate. The combined organic layer was washed with water, dried, filtered, and concentrated to afford 6-acryloyloxyhexanoic acid. 1H NMR (CDCl3, 500 MHz) δ 1.46 (m, 2H), 1.70 (m, 4H), 2.37 (t, J=7.3 Hz, 2H), 4.17 (t, J=6.4 Hz, 2H), 5.82 (d, J=10.4 Hz, 1H), 6.12 (dd, J=17.3, 10.5 Hz, 1H), 6.39 (d, J=17.3 Hz, 1H), 11.59 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07914700B2
Source datasetuspto-grants-2011_03
ORD IDord-10a2bc1a923c4c2cb7ee660e3d52ed8a
Source noteuspto-grants-2011_03