HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968754Generated: October 29, 2026
Water → {3-Chloro-8-[(dimethylamino)methyl]naphthalen-2-yl}methanol
https://huagongshe.com/reaction/1968754
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 3-Chloro-8-dimethylaminomethyl-naphthalene-2-carboxylic acid ethyl ester | HCID 66882796 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {3-Chloro-8-[(dimethylamino)methyl]naphthalen-2-yl}methanol | HCID 66882407 | 96% |
Reaction Steps
Diisobutylaluminium hydride (1M in THF, 4.2 ml, 4.1 mmol, 9.0 equiv) was added to a solution of 3-chloro-8-dimethylaminomethyl-naphthalene-2-carboxylic acid ethyl ester (133 mg, 0.46 mmol) in 3.2 ml anhydrous THF at 0° C. After 15 minutes at 0° C., TLC analysis revealed complete conversion of starting material. Water (30 ml) was added, and the mixture was extracted with EtOAc (2×100 ml). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification via flash chromatography (gradient of CH2Cl2/MeOH 97:3 to 90:10) afforded the title compound (109 mg, 96%, mixture of 2 regioisomers) as a colorless oil. Data for (3-chloro-8-dimethylaminomethyl-naphthalen-2-yl-methanol: 1H NMR (400 MHz, CDCl3): δ=8.36 (s, 1H), 7.85 (s, 1H), 7.74 (dd, J=7.1/1.9 Hz, 1H), 7.44-7.39 (m, 2H), 4.94 (s, 2H), 4.06 (s, 2H), 2.45 (s, 6H). MS (ES+): 250 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426440B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-b0b2b98f074e4edc902befd4b8eb48b0 |
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| Source note | uspto-grants-2013_04 |
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