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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629818Generated: October 31, 2026

1-Chloro-N,N-2-trimethylpropenylamine → HCID 118435542, compound

https://huagongshe.com/reaction/629818

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
ReactantHCID 118435603HCID 118435603—
SolventDichloromethaneHCID 6344—
ProductHCID 118435542HCID 118435542—

Reaction Steps

1-Chloro-N,N,2-trimethylprop-1-en-1-amine (Ghosez's reagent, 7.85 mL, 59.3 mmol) was added drop-wise to a solution of C5 (9.30 g, 19.8 mmol) in dichloromethane (200 mL). After 1 hour at room temperature, the reaction mixture was partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel chromatography (Gradient: 0% to 100% ethyl acetate in heptane) provided the product as a solid. Yield: 6.90 g, 15.2 mmol, 77%. LCMS m/z 452.1, 454.1 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 13.69 (br s, 1H), 8.38-8.43 (m, 2H), 7.64-7.70 (m, 1H), 7.54-7.60 (m, 2H), 7.34 (s, 1H), 4.45 (d, J=12.5 Hz, 1H), 3.93 (d, J=12.5 Hz, 1H), 3.74-3.83 (m, 1H), 3.28-3.36 (m, 1H), 3.23 (dd, J=13.5, 4.0 Hz, 1H), 2.77 (dd, J=13.5, 2.8 Hz, 1H), 1.66-1.82 (m, 2H), 1.32 (d, J=6.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315520B2
Source datasetuspto-grants-2016_04
ORD IDord-5f0ecba10e4e43639fc9fc114c851c32
Source noteuspto-grants-2016_04