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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259608Generated: October 30, 2026

Triethylamine → HCID 57149177, compound

https://huagongshe.com/reaction/2259608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 131719218HCID 131719218—
SolventDichloromethaneHCID 6344—
ProductHCID 57149177HCID 57149177—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Chlorosuccinimide (1.0 g, 0.007 mol) was added to a mixture of 2.7 g (0.007 mol) of the product from Step D, 0.75 g of 3A molecular sieves and 120 mL of methylene chloride. The resulting mixture was cooled to 0° C. and was treated with a solution of 1.3 mL of triethylamine and 60 mL of methylene chloride. The resulting mixture was stirred at room temperature for 4 h and then decanted into 100 mL of water. The aqueous layer was extracted with two 50 mL portions of methylene chloride and the combined organic layers were washed with water and saturated sodium bicarbonate solution, dried over anhydrous magnesium sulfate and concentrated to give 2.9 g of a brown oil. Flash chromatography on silica gel using 1:3 hexanes-EtOAc afforded 1.0 g of a light yellow oil. 200 MHz 1H NMR (CDCl3): δ1.36 (t, 6H), 3.55 (dd, 1H), 3.9 (d, 1H), 4.1-14.3 (m, 5H), 4.60 (d, 1H), 5.15-5.3 (m, 2H), 5.90-6.05 (m, 1H), 6.9-7.0 (m, 2H), 7.78 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05474998
Source datasetuspto-grants-1995_12
ORD IDord-51a895594b604e999d7a03c1df71f10d
Source noteuspto-grants-1995_12