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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042898Generated: October 30, 2026

Sodium Thiosulfate → HCID 21771543, compound

https://huagongshe.com/reaction/2042898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantIodine chlorideHCID 24640—
ReactantN-[(2H-1,3-Benzodioxol-5-yl)methyl]ethanimidic acidHCID 290549—
SolventDichloromethaneHCID 6344—
ProductHCID 21771543HCID 2177154338%

Reaction Steps

N-(benzo[d][1,3]dioxol-5-ylmethyl)acetamide (9.24 g, 47.9 mmol) was added to 1.0 M solution of iodine monochloride in methylene chloride (80 mL). The mixture was stirred at room temperature for 2 hours, and then the mixture was poured into 10% Na2S2O3 and stirred until the red color faded. It was then extracted with CH2Cl2 and the organic layer was washed with water and brine, dried and concentrated to get the crude product which was purified by column chromatography (mobile phase: petroleum/methylene chloride=1/19) to give N-((6-iodobenzo[d][1,3]dioxol-5-yl)methyl)acetamide compound as a white solid (5.82 g, 38%). LC-MS: 320 [M+1]+. 1H-NMR (DMSO-d6): δ 1.89 (s, 3H), 4.11 (d, 2H, J=6.0 Hz), 6.04 (s, 2H), 7.07 (s, 1H), 7.37 (s, 1H), 8.28 (t, 1H, J=6.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586605B2
Source datasetuspto-grants-2013_11
ORD IDord-a58eb456274a4d1f8598ce3fcec099bd
Source noteuspto-grants-2013_11