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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961497Generated: October 30, 2026

Water → HCID 67355942, compound

https://huagongshe.com/reaction/1961497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-ButylamineHCID 6385—
ReactantHCID 86623447HCID 86623447—
SolventHexaneHCID 8058—
ProductHCID 67355942HCID 6735594294%

Reaction Conditions

Temperature37.5 °C

Reaction Steps

A 3-neck, 3 L, round-bottom flask was equipped with an over-head stirrer, thermometer, and a pressure-equalizing dropping-funnel was charged with the solution of 4-benzyloxy-3-iodo-benzenesulfonyl chloride. The flask immersed in a cold water bath (Tint=22° C.) and tert-butylamine (90.1 g, 0.710 mol, 2.1 eq) was added drop-wise (Tint no change). The resulting reaction mixture was stirred overnight at the ambient water-bath temperature. After 17 h, the reaction mixture was worked-up and the organic layer was separated and concentrated to approx. ⅓ (˜500 mL) of its original volume at which point the product started to precipitate. The reaction mixture was warmed to 35-40° C. at atmospheric pressure till the solids had re-dissolved. The solution was then allowed to cool, with gentle stirring, to room temperature. Within 2 days a white precipitate had formed. The suspension was stirred vigorously while hexane (1.5 L) was slowly added, then stirred overnight, and then cooled in an ice-bath for 1-2 h The precipitate was collected by filtration and washed with hexane, dried, first under suction to give 4-benzyloxy-N-tert-butyl-3-iodo-benzenesulfonamide (238, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415328B2
Source datasetuspto-grants-2013_04
ORD IDord-a24e2fe66dbf4ec6bbadcfe0f8e205b7
Source noteuspto-grants-2013_04