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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737455Generated: November 1, 2026

Benzoyl chloride → HCID 21842644, compound

https://huagongshe.com/reaction/1737455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 21842589HCID 21842589—
SolventDichloromethaneHCID 6344—
ProductHCID 21842644HCID 2184264493.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

N,N-Diisopropylethylamine (0.352 mL, 261 mg, 2.02 mmol) and 5-(methylamino)-3-phenylpentan-1-ol (300 mg, 1.68 mmol) from Example 180, Step B, were dissolved in 4.0 mL of dichloromethane. The solution was cooled to 0° C., benzoyl chloride (0.205 mL, 248 mg, 1.77 mmol) was added dropwise, and the mixture was stirred for an additional 30 min. The mixture was then partitioned between 15 mL of dichloromethane and 15 mL of saturated aqueous sodium bicarbonate solution. The aqueous layer was extracted with 2×15 mL of dichloromethane. The combined organic extracts were washed with 20 mL of brine, dried over sodium sulfate, and evaporated. The crude product was purified by flash column chromatography on silica gel, eluting with 10% ethyl acetate in dichloromethane, to give 467 mg of the title compound. 1NMR (400 MHz, CD3OD) was complicated by the presence of a mixture of rotamers: δ 7.45-7.06 (m, 9H), 6.97 (d, 1H, J=8 Hz), 3.53-3.23 (m, 2H), 3.17-3.00 (m, 2H), 3.02 and 2.85 (two singlets, 3H), 2.88-2.78 and 2.57-2.49 (two multiplets, 1H), 2.07-1.64 (m, 4H). Mass spectrum (ESI): m/z=298 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962462
Source datasetuspto-grants-1999_10
ORD IDord-13fcaeb613b443f0a1590838dcab50ea
Source noteuspto-grants-1999_10