HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426064Generated: October 31, 2026
3-Chloro-5-fluoro-2-methoxybenzaldehyde → HCID 58707255, compound
https://huagongshe.com/reaction/2426064
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-5-fluoro-2-methoxybenzaldehyde | HCID 13093560 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 58707255 | HCID 58707255 | 98% |
Reaction Steps
To a stirred solution of 5-Fluoro-2-methoxy-3-chlorobenzaldehyde (2.0 g, 11.0 mmol) in dry diethyl ether (40 mL) at 0° C. was added methylmagnesium bromide of 3.0 M in ether (8.8 mL, 27.12 mmol). The reaction mixture was brought to room temperature and was stirred for 30 min then refluxed for 3 hours. It was then cooled to 0° C. and quenched by adding saturated aqueous NH4Cl. The two liquid layers were separated. The aqueous layer was extracted with ether. The combined organic layers were washed with water, dried, and concentrated to the crude compound which was purified by silica gel column (10-25% ethyl acetate in hexanes) to afford 1-(5-Fluoro-2-methoxy-3-chlorophenyl)ethanol (2.1 g, 98%): 1H NMR (400 MHz, CDCl3): δ 7.12 (dd, 1H), 7.04 (dd, 1H), 5.19 (m, 1H), 3.84 (s, 3H), 2.18 (bs, 1H), 1.43 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968538B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-69309dc6c7694280adbf2b355e520cad |
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| Source note | uspto-grants-2011_06 |
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