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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708567Generated: November 2, 2026

Triethylamine → HCID 19048401, compound

https://huagongshe.com/reaction/1708567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 10920154HCID 10920154—
SolventDichloromethaneHCID 6344—
ProductHCID 19048401HCID 19048401—

Reaction Steps

To a stirred solution of N,N'-bis[2,3bis (acetyloxy)propyl]-2,4,6-triiodo-5-[[(tetrahydro-2-furanyl)carbonyl]amino]-1,3-benzenedicarboxamide (0.25 g, 0.26 mmol) (the title compound of Example 4) in dry CH2Cl2 (5 mL) was added triethyl amine (0.01 mL). The solution was cooled to 0°-5° , and to this was added dropwise a solution of dimethylboron bromide in CH2Cl2 (0.12 g, 0.5 mL/2 mMol solution in CH2Cl2). After stirring the mixture at 0°-5° for 6-8 hours, the mixture was added to a vigorously stirred solution of aqueous saturated sodium bicarbonate (5 mL). After stirring for 5 minutes, ethyl acetate (50 mL) and water (10 mL) were added. The organic layer was separated, washed with water, dried over anhydrous sodium sulfate, and concentrated in vacuo to yield the omega-bromo-alpha-hydroxypentanoyl anilide as an off-white fluffy solid (260 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359077
Source datasetuspto-grants-1994_10
ORD IDord-6f0f51e3177447f1a1166f1e8506711e
Source noteuspto-grants-1994_10