HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765814Generated: November 1, 2026
Phenol, 3-(1,1-dimethylethyl)- → 4-tert-Butyl-2-hydroxybenzaldehyde
https://huagongshe.com/reaction/1765814
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenol, 3-(1,1-dimethylethyl)- | HCID 11450 | — |
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-tert-Butyl-2-hydroxybenzaldehyde | HCID 13765272 | 77% |
Reaction Steps
A stirred, cooled (ice bath) solution of 3-tert-butyl phenol (1.5 g, 10 mmol) in anhydrous dichloromethane was treated with titanium tetrachloride (1.86 mL, 17 mmol) followed by α,α-dichloromethyl ether (0.9 mL, 20 mmol). The reaction was allowed to warm to ambient temperature over 1 h, quenched cautiously with ice and water and extracted with dichloromethane. The organic extract was washed with water and brine, dried over sodium sulfate, filtered and evaporated in vacuo to a residue that was subjected to flash column chromatography using 2–2.5% ethyl acetate in hexane as the eluent to afford the title compound (1.37 g, 77%). 1H NMR (300 MHz, CDCl3): δ 11.02 (s, 1H), 9.81 (s, 1H), 7.45 (d, J=8.2 Hz, 1H), 7.03 (dd, J=8.2, 1.7 Hz, 1H), 6.99 (d, J=1.7 Hz, 1H), 1.31 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07226951B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-06fd64353b804678b56c5a44c67377bf |
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| Source note | uspto-grants-2007_06 |
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