HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404199Generated: October 31, 2026
Methane, dichloromethoxy- → 6-(4-Tert-butyl-cyclohexyloxy)-8-methyl-naphthalene-2-carbaldehyde
https://huagongshe.com/reaction/2404199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 3-(4-Tert-butyl-cyclohexyloxy)-1-methyl-naphthalene | HCID 68172797 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-(4-Tert-butyl-cyclohexyloxy)-8-methyl-naphthalene-2-carbaldehyde | HCID 86668429 | 98.6% |
Reaction Steps
To a mixture of 3-(4-tert-butyl-cyclohexyloxy)-1-methyl-naphthalene (450 mg, 1.5 mmol) in 1,2-dichloroethane (9 mL) was added tin tetrachloride (236 uL, 2 mmol) at 0° C. After stirred at 0° C. for 1 hr, dichloromethyl methyl ether (183 uL, 2 mmol) was added. The solution was stirred at 0° C. for 1 hr and then warmed to room temperature. The mixture was added ice water and stirred for 1 hr, then the dark solution was diluted with dichloromethane and washed with water. The organic phase was washed with sodium bicarbonate aqueous, and dried over MgSO4. The drying agent was filtered off and the solvent was concentrated to dryness to give dark solid product (0.48 g, yield: 97%). ESI-MS: 325.20 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802659B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-c4eff4b594a346c0a18c8160f707311f |
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| Source note | uspto-grants-2014_08 |
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