HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732839Generated: October 29, 2026
HCID 86737367, compound → HCID 86737369, compound
https://huagongshe.com/reaction/1732839
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86737367 | HCID 86737367 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86737369 | HCID 86737369 | 97% |
Reaction Steps
Methyllithium (63.3 ml, 0.0918 mol, 1.45 M in ether) is added dropwise to a solution of the aldehyde (2S*, 3R*)-3-benzyloxy-1,1-ethylenedioxy-2-methyl-2-(4'-oxobutyl)-cyclohexane (25.4 g, 0.0765 mol) in ether (1000 ml) at 0° C. in a nitrogen atmosphere. The cooling bath is removed and the mixture is stirred for 0.5 hours at ambient temperature. The mixture is then poured into a cold saturated sodium chloride solution (500 ml). The ether phase is separated and the aqueous phase is extracted with ether (3×100 ml). The ether phases are combined, dried (MgSO4) and the solvent is removed at reduced pressure. The crude product (27.1 g) is chromatographed on SilicAR CC-7 (300 g, Millinckrodt) in hexane. Elution with 10% ethyl acetate/hexane gives (2S*, 3R*)-3-benzyloxy-1,1-ethylenedioxy-2-methyl-2-(4'-hydroxypentyl)-cyclohexane as a colorless oil (25.8 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04239689 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-0da47d08075a4e64a2d3e79c9ae46894 |
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| Source note | uspto-grants-1980_12 |
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