HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926197Generated: November 2, 2026
tert-Butanol → 1-(1-Chloro-3-methyl-naphthalen-2-yl)-ethane-1,2-diol
https://huagongshe.com/reaction/926197
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 1-Chloro-3-methyl-2-vinylnaphthalene | HCID 67126076 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(1-Chloro-3-methyl-naphthalen-2-yl)-ethane-1,2-diol | HCID 77184474 | — |
Reaction Steps
A biphasic mixture of AD mix-α (6.907 g) in tert-butanol (24.5 mL)/H2O (24.5 mL) was cooled to 0° C. and 1-chloro-3-methyl-2-vinyl-naphthalene (1.00 g, 4.93 mmol) was added. The reaction mixture was stirred for 8 h at 0° C. Sodium sulfite (7.4 g) was added at 0° C. and the reaction was stirred for 40 minutes to give a white mixture. The mixture was diluted with dichloromethane and H2O. The mixture was extracted with dichloromethane (3×) and the combined organic layer was dried (MgSO4), filtered, concentrated and purified by flash column chromatography (silica gel, 0 to 100% ethyl acetate/hexanes) to give 1-(1-chloro-3-methyl-naphthalen-2-yl)-ethane-1,2-diol. 1H NMR (400 MHz, CDCl3) δ 8.27 (d, J=8.2 Hz, 1H), 7.72 (d, J=7.8 Hz, 1H), 7.57 (s, 1H), 7.56-7.47 (m, 2H), 5.70 (dd, J=9.4, 3.9 Hz, 1H), 4.11 (dd, J=10.5, 10.5 Hz, 1H), 3.80 (dd, J=11.6, 3.9 Hz, 1H), 2.66 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284323B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-7904829a49a242f6b99b0afa8dd5a37a |
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| Source note | uspto-grants-2016_03 |
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