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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201624Generated: October 28, 2026

Triethylamine → HCID 59378874, compound

https://huagongshe.com/reaction/2201624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHeptaneHCID 8900—
Reactantm-FluorobenzenethiolHCID 75710—
Reactant6-Fluoro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 14915116—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 59378874HCID 5937887492.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 6-fluoro-3,4-dihydro-2H-naphthalen-1-one (3.64 kg) and 3-fluorothiophenol (2.80 kg), in anhydrous NMP (7.7 kg) was treated with triethylamine (2.26 kg). After a mild exotherm had subsided, the mixture was heated for 20 hours at 90° C. The mixture was cooled to about 25° C. and diluted with water (30 L) and heptane (10 kg). The mixture was agitated for 12 hours and then filtered. The filter cake was washed with water and dried at 60° C. under vacuum to afford 6-(3-fluorophenylsulfanyl)-3,4-dihydro-2H-naphthalen-1-one (5.52 kg): MP=66.2-66.7° C.; MS (M+1)=273; H1 NMR (300 MHz): δ ppm (CDCl3): 2.10 (2H, m, J=6.03, 6.40 Hz), 2.62 (2H, dd, J=6.03, 5.75 Hz) 2.87 (2H, t, J=6.03), 7.03 (1H, tdd, J=1.13, 2.64, 8.29 Hz), 7.08-7.16 (2H, m), 7.22 (1H, dt, J=1.13, 8.29 Hz), 7.31 (1H, q, 8.29 Hz), 7.35 (1H, dd, J=5.65, 7.91 Hz) 7.92 (1H, d, J=7.91 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365494B2
Source datasetuspto-grants-2016_06
ORD IDord-662e939fcfa640349aff340ca3cf291b
Source noteuspto-grants-2016_06