HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843289Generated: November 2, 2026
4-Chlorophenyl Isocyanate → HCID 60163512, compound
https://huagongshe.com/reaction/1843289
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorophenyl Isocyanate | HCID 7693 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Benzyl-1,2,3,4-tetrahydroquinolin-7-ol | HCID 21864936 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 60163512 | HCID 60163512 | — |
Reaction Steps
A mixture of 1-benzyl-1,2,3,4-tetrahydroquinolin-7-ol (800 mg, 3.34 mM) and triethylamine (1.5 mL) in dry tetrahydrofuran (THF, 5 ml) was stirred for half an hour under nitrogen atmosphere at room temperature (35° C.). To the stirred reaction mixture, 4-chiorophenyl isocyanate (641 mg/ml, 5.01 mM) was added at once and then the reaction mixture was further stirred for 72 hours under N2 atmosphere at RT. The reaction mixture was concentrated under vacuum and then was added distilled water (15 mL) followed by the extraction with ether (3×15 mL). The ether layer was dried over sodium sulphate and concentrated under vacuum to afford the crude product, which was finally crystallized with methanol-ether (1:6) to give 8f as solid. Yield: 1.06 g, 80.70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946261B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-07b184649a4d4a529bcc033bd9892f5d |
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| Source note | uspto-grants-2015_02 |
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