HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057644Generated: November 3, 2026
Pentane → 2-({9-[(5-Chloro-1-benzothiophen-3-yl)methyl]-9H-carbazol-4-yl}oxy)acetonitrile
https://huagongshe.com/reaction/1057644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pentane | HCID 8003 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(Bromomethyl)-5-chloro-1-benzothiophene | HCID 2779857 | — |
| Reactant | (9H-Carbazol-4-yloxy)acetonitrile | HCID 18671668 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-({9-[(5-Chloro-1-benzothiophen-3-yl)methyl]-9H-carbazol-4-yl}oxy)acetonitrile | HCID 18671680 | 56% |
Reaction Steps
2-(9H-Carbazol-4-yloxy)acetonitrile (0.146 g, 0.66 mmol)) is added to a slurry of pentane-washed NaH (0.0441 g, 0.0011 mol) in DMF (1 mL) and allowed to stir for 20 min at room temperature. 3-(Bromomethyl)-5-chlorobenzothiophene (0.229 g, 0.88 mmol) is added and after stirring for 1 h the mixture is partitioned between ethyl acetate and water. The combined organic layers are dried over magnesium sulfate and concentrated to an oil. The oil is chromatographed on silica gel (75 mL) using ethyl acetate/hexane (20/80) and solids are precipitated using dichloromethane/hexane to give 0.148 g (56%) of the title compound; MS (ESI+) for C23H15ClN2OS m/z 425.2 (M+Na); IR (drift) 1581, 1460, 1439, 1332, 1279, 1232, 1221, 1155, 1148, 1115, 1079, 833, 780, 752, 717 cm−1; 1H NMR (CDCl3) δ5.10, 5.70, 6.72, 6.80, 7.12, 7.28-7.47, 7.80, 7.87, 8.36. Anal. Calcd for C23H15ClN2OS: C, 68.57; H, 3.75; N, 6.95. Found: C, 68.87; H, 4.22; N, 6.56.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06514968B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-7666177effb844e4b4cf9e1ff35fb083 |
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| Source note | uspto-grants-2003_02 |
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