HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409486Generated: October 28, 2026
Methanol → Cyclohexanecarboxylic acid, 4-(hydroxymethyl)-, methyl ester
https://huagongshe.com/reaction/409486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Benzyloxymethyl-cyclohexanecarbaldehyde | HCID 18667240 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Cyclohexanecarboxylic acid, 4-(hydroxymethyl)-, methyl ester | HCID 11073869 | — |
| Product | 4-Benzyloxymethyl-cyclohexanecarboxylic acid methyl ester | HCID 57686688 | — |
Reaction Steps
4-Benzyloxymethyl-cyclohexanecarbaldehyde (1.70 g, 2.0 mmol) is dissolved in acetic acid (0.24 mL) and 2 mL of MeOH. The reaction mixture is cooled to 0-5° C. and stirred while 10% NaOCl solution (2.5 mL, 4 mmol) is added dropwise over 20 minutes. The cooling bath is removed and the mixture is allowed to come to room temperature. After addition of saturated aqueous NaHCO3, the aqueous layer is extracted with EtOAc. The combined organic layer (dried with MgSO4) is concentrated. The desired product, 4-benzyloxymethyl-cyclohexanecarboxylic acid methyl ester, is obtained (343 mg, 65%) after purification using silica gel column chromatography (eluent: EtOAc/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759365B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-d7f62e37ac8f447daf4b1c4c90f52f06 |
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| Source note | uspto-grants-2014_06 |
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