HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28754Generated: October 25, 2026
Ethyl Acetate → 5-(2-Benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester
https://huagongshe.com/reaction/28754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 5-(2-Benzyloxy-ethyl)-2-hydroxy-cyclohexanecarboxylic acid methyl ester | HCID 23549539 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-(2-Benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester | HCID 23549538 | — |
Reaction Steps
A solution of 5-(2-benzyloxy-ethyl)-2-hydroxy-cyclohexanecarboxylic acid methyl ester (Intermediate R2, 0.72 g, 2.48 mmol) in pyridine (10 mL) was treated with SOCl2 (0.73 mL, 12.4 mmol) at −20° C. The mixture was allowed to react for 15 m and was then warmed to 55° C. for 16 h. The solvents were removed under vacuum and the residue was diluted in ether at 0° C. The solution was quenched with water, washed with 1M HCl, 5% NaOH and brine. The organic material was dried over MgSO4 filtered and freed of solvent. The mixture was diluted with benzene and water was removed by azeotropic distillation under vacuum. The residue was dissolved in benzene (15 mL) and DBU (0.76 mL, 5 mmol) was added. The mixture was reacted for 30 m at rt. After work-up and chromatography on SiO2 with 20% EtOAc:Hx 5-(2-benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester (Intermediate R3) was isolated 0.56 g (82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07419994B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-3e4af5401fd84d3f9164346abaccb2fb |
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| Source note | uspto-grants-2008_09 |
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