HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729774Generated: October 31, 2026
Dichloromethane → 1,2,3,4-Tetrahydro-8-methyl-1-naphthalenemethanol
https://huagongshe.com/reaction/729774
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 12778763 | HCID 12778763 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2,3,4-Tetrahydro-8-methyl-1-naphthalenemethanol | HCID 11805271 | — |
Reaction Steps
8-Methyl-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid (J. Org. Chem. 1982, 47, 2590-2593) (0.066 g, 0.34 mmol) was dissolved in tetrahydrofuran (3 mL). To the solution was then added at 0° C. a 1.0M solution of borane-methyl sulfide complex in dichloromethane (0.7 mL, 0.69 mmol). The reaction mixture was stirred at room temperature for 15 minutes, refluxed for 2 hrs, then cooled down to 0° C. and quenched with methanol. The solvent was then evaporated in vacuo to yield a crude oil. The crude oil was partitioned with water and diethyl ether. The organic layer was dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield crude (8-methyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-methanol as an oil which was used directly to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582649B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-0899306fd8b74cb4a68aec38acf29d53 |
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| Source note | uspto-grants-2009_09 |
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