HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843286Generated: November 1, 2026
Triethylamine → 1-Benzyl-1,2,3,4-tetrahydroquinolin-7-yl 2-fluorophenylcarbamate
https://huagongshe.com/reaction/1843286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluorophenyl isocyanate | HCID 85588 | — |
| Reactant | 1-Benzyl-1,2,3,4-tetrahydroquinolin-7-ol | HCID 21864936 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzyl-1,2,3,4-tetrahydroquinolin-7-yl 2-fluorophenylcarbamate | HCID 60163506 | — |
Reaction Steps
A mixture of 1-benzyl-1,2,3,4-tetrahydroquinolin-7-ol (805 mg, 3.36 mM) and triethylamine (0.6 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, 2-fluorophenyl isocyanate (565 mg/ml, 5.04 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 chromatographed using chloroform-hexane (1:9) to give 8c as oil. Yield: 1.02 g, 80.56%.
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-67b555340d0f4b5e8e3b126b1eee5e6a |
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| Source note | uspto-grants-2015_02 |
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