HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482442Generated: October 26, 2026
Methacrylic Acid → 6-Hydroxyhexyl Methacrylate (stabilized with MEHQ)
https://huagongshe.com/reaction/1482442
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | 1,6-Hexanediol | HCID 12374 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Hydroxyhexyl Methacrylate (stabilized with MEHQ) | HCID 9794090 | 67.7% |
Reaction Steps
1,6-Hexanediol (1000.00 g, 8.46 mol, Sigma-Aldrich) was placed in a 1-liter 3-neck flask equipped with a mechanical stirrer and a narrow tube blowing dry air into the flask. The solid diol was heated to 90° C., at which temperature all the solid melted. With continuous stirring, p-toluenesulfonic acid crystals (18.95 g, 0.11 mol) followed by BHT (2.42 g, 0.011 mol) and methacrylic acid (728.49.02 g, 8.46 mol). Heating at 90° C. with stirring was continued for 5 hours during which time vacuum was applied using tap water aspirator for 5-10 minutes after each half-hour reaction time. The heat was turned off and the reaction mixture was cooled to room temperature. The viscous liquid obtained was washed with 10% aqueous sodium carbonate twice (2×240 ml), followed by washing with water (2×240 ml), and finally with 100 ml of saturated NaCl aqueous solution. The obtained oil was dried using anhydrous Na2SO4 then isolated by vacuum filtration to give 1067 g (67.70%) of 6-hydroxyhexyl methacrylate, a yellow oil. This desired product was formed along with 15-18% of 1,6-bis(methacryloyloxyhexane). Chemical characterization was by NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09414995B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-94a8d83118074af88426316a15adadf3 |
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| Source note | uspto-grants-2016_08 |
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