HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426056Generated: November 2, 2026
6-Chlorobenzo[d][1,3]dioxole-4-carbaldehyde → 1-(5-Chlorobenzo[d][1,3]dioxol-7-yl)ethanol
https://huagongshe.com/reaction/2426056
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Chlorobenzo[d][1,3]dioxole-4-carbaldehyde | HCID 58707311 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(5-Chlorobenzo[d][1,3]dioxol-7-yl)ethanol | HCID 58707314 | — |
Reaction Steps
6-Chlorobenzo[d][1,3]dioxole-4-carbaldehyde (147.0 mg, 0.79 mmol) was dissolved in 6 mL of diethyl ether and cooled to 0° C. MeMgBr (0.60 mL, 1.99 mmol) was added to the solution and the ice bath was removed. The reaction was allowed to stir at rt for 10 min. and at reflux for 30 min. The reaction was cooled to 0° C. and 10 mL of sat NH4Cl were added to quench the reaction. The diethyl ether layer was separated and washed with water (10 mL×2). The organic layer was dried over Na2SO4 and the solvent was removed by rotary evaporation to collect the desired product (155.0 mg, 98%). 1H NMR (400 MHz, CDCl3): δ 6.90 (d, 1H), 6.75 (d, 1H), 6.01 (d, 2H), 4.96 (m, 1H), 1.50 (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-4423612db6774ff794c0600a5a8d7a27 |
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| Source note | uspto-grants-2011_06 |
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