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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421449Generated: October 29, 2026

Ammonium Hydroxide → HCID 66658201, compound

https://huagongshe.com/reaction/421449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 86636774HCID 86636774—
SolventAcetonitrileHCID 6342—
ProductHCID 66658201HCID 6665820184%

Reaction Conditions

Temperature0 °C

Reaction Steps

Concentrated aqueous ammonium hydroxide solution (3 mL) was added to a solution of Boc-4-(methanesulfonylamino-methyl)-2-nitro-thiophene-3-sulfonyl chloride (3.30 g, 7.59 mmol) in acetonitrile (90 mL) at 0° C. The mixture was stirred at 0° C. for 45 min, and then was partitioned between half-saturated aqueous sodium bicarbonate solution (150 mL) and ethyl acetate (2×150 mL). The combined organic layers were dried over sodium sulfate, filtered and were concentrated in vacuo. Purification of the residue by flash column chromatography (Teledyne Isco RediSep column; 20-90% ethyl acetate in hexanes) afforded the desired product, Boc-4-(methanesulfonylamino-methyl)-2-nitro-thiophene-3-sulfonic acid amide (2.64 g, 6.35 mmol, 84%), as a yellow solid. 1H NMR (400 MHz, CDCl3) δ: 1.54 (9H, s), 3.35 (3H, s), 5.12 (2H, s), 5.81 (2H, bs), 7.61 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097613B2
Source datasetuspto-grants-2012_01
ORD IDord-d7c27d16a3a64bb58bc6f8bd8e2618e5
Source noteuspto-grants-2012_01