HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712047Generated: October 25, 2026
Methyl Acrylate → Methyl-2-methoxy-4-[(trimethylsilyl)oxy]cyclohex-3-ene-1-carboxylate
https://huagongshe.com/reaction/712047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | 1-Methoxy-3-trimethylsilyloxy-1,3-butadiene | HCID 101051 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl-2-methoxy-4-[(trimethylsilyl)oxy]cyclohex-3-ene-1-carboxylate | HCID 15496370 | — |
Reaction Steps
A mixture of methyl acrylate (5.23 mL, 58.0 mmol) and 1-methoxy-3-(trimethylsiloxy)-1,3-butadiene (from Aldrich, 10.0 g, 58.0 mmol) in toluene (100 mL) was heated at 80° C. for 2 d. The reaction solution was concentrated and purified on silica gel column to give the desired product as a mixture of trans- and cis-isomers (8.3 g, 55%). 1H NMR (500 MHz, CDCl3) δ 5.16 (1H, m), 4.97 (1H, m), 4.22 (1H, m), 4.08 (1H, m), 3.68 (3H, s), 3.67 (3H, s), 3.32 (3H, s), 3.24 (3H, s), 2.59 (1H, m), 2.51 (1H, m), 1.80-2.14 (8H, m), 0.18 (18H, s) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181271B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-0b335b29582d49b5abad380ade4b8dff |
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| Source note | uspto-grants-2015_11 |
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