HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695259Generated: October 30, 2026
2-Chloro-6-methylphenol → HCID 67246220, compound
https://huagongshe.com/reaction/1695259
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-6-methylphenol | HCID 6898 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | tert-Butyldimethylsilane | HCID 5072427 | — |
| Reactant | HCID 57999891 | HCID 57999891 | — |
| Reactant | HCID 67246834 | HCID 67246834 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67246220 | HCID 67246220 | — |
Reaction Steps
Triethyl amine (36 mL, 0.263 mol) was added to a solution of (2-bromomethyl-6-chloro-phenoxy)-tert-butyl-dimethyl-silane (72 g, 0.214 mol) [prepared from 6-chloro cresol by protecting the hydroxy group with t-butyldimethylsilane followed by bromination using N-bromosuccinimide] and compound of Example 1f (43 g, 0.164 mol) in chloroform (600 mL) at 5° C. over a period of 20 min. The reaction mixture was stirred at 25° C. for 30 min. The reaction mixture was washed with water (2×200 mL) and brine (100 mL). The solvent was removed under reduced pressure and to the oily mass obtained, methanol (300 mL) was added with stirring. The crystalline solid obtained was filtered, washed with methanol and dried to obtain the title compound. Yield: 70 g, (83%); 1H NMR (CDCl3, 300 MHz): δ 0.28 (s, 6H, 2CH3), 1.03 (s, 9H, 3CH3), 2.45 (s, 3H, CH3), 3.89 (s, 3H, OCH3), 4.19 (s, 2H, CH2), 6.89 (t, 1H, Ar), 7.24 (t, 1H, Ar), 7.32 (d, 1H, Ar), 7.61 (s, 1H, Ar), 7.69 (s, 1H, Ar); MS: m/e (ES−) 515 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163730B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-7165219f102648d2b5621f1737dc1d82 |
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| Source note | uspto-grants-2012_04 |
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