HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432854Generated: October 27, 2026
6-Chloro-2-tetralone → 6-Chloro-2-methyl-1,2,3,4-tetrahydronaphthalene-2-ol
https://huagongshe.com/reaction/1432854
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Chloro-2-tetralone | HCID 4456139 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-2-methyl-1,2,3,4-tetrahydronaphthalene-2-ol | HCID 53810915 | — |
Reaction Steps
To a solution of TiCl4 (95 mL, 1M in toluene) at −45° C. is added a solution of CH3MgBr (4.2 mL 3M in THF). The solution is stirred for 20 minutes. After this time, 6-chloro-3,4-dihydro-1H-naphthalene-2-one (11.3 g, 63 mmol) in 80 mL of CH2Cl2 is added dropwise over 15 minutes. The reaction is stirred for an additional 15 min at −45° C. The solution is warmed to 0° C. After 2 h, the solution is diluted with H2O and CH2Cl2. The organic layer is dried over MgSO4, filtered and concentrated. The title compound is obtained as an oil (11.3 g, 57.5 mmol). 1H NMR (CDCl3, 300 MHz) δ7.10 (m, 2H), 6.97 (m, 1H), 3.02 (m, 2H), 2.80 (s, 3H), 1.85 (m, 2H), 1.80 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-fc812cd494c046c4bcda191920a4bb10 |
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| Source note | uspto-grants-2009_11 |
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