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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476010Generated: October 31, 2026

2-Methanesulfonylbenzene-1-sulfonyl chloride → 1-({[(Tert-butoxy)carbonyl]({[(1,3-diethoxypropan-2-yl)oxy]carbonyl}oxy)-amino}sulfonyl)-2-methanesulfonylbenzene

https://huagongshe.com/reaction/1476010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735178—
Reactant2-{[({[(tert-Butoxy)carbonyl]amino}oxy)carbonyl]oxy}-1,3-diethoxypropaneHCID 86654183—
Product1-({[(Tert-butoxy)carbonyl]({[(1,3-diethoxypropan-2-yl)oxy]carbonyl}oxy)-amino}sulfonyl)-2-methanesulfonylbenzeneHCID 53241814—

Reaction Steps

1-({[(tert-Butoxy)carbonyl]({[(1,3-diethoxypropan-2-yl)oxy]carbonyl}oxy)-amino}sulfonyl)-2-methanesulfonylbenzene (102) is prepared from 2-{[({[(tert-butoxy)carbonyl]amino}oxy)carbonyl]oxy}-1,3-diethoxypropane and 2-methylsulfonyl benzene sulfonyl chloride according to Scheme 11. (2.3 g, 47%), 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 8.39 (2H, ddd, 12.2, 7.5, 1.5 Hz), 7.84 (2H, m), 5.06 (1H, quin, 5.1 Hz), 3.68 (4H, t, 4.9 Hz), 3.48-3.61 (4H, m), 1.43 (9H, s), 1.27 (3H, t, 7.2 Hz), 1.19 (3H, t, 6.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018411B2
Source datasetuspto-grants-2015_04
ORD IDord-8a25622818f242cf81d6fe8379e7ef4e
Source noteuspto-grants-2015_04