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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170109Generated: October 26, 2026

Sodium Hydroxide → 3-[(1-tert-Butoxycarbonyl-cyclobutylmethyl)-sulfamoyl]-benzoic acid

https://huagongshe.com/reaction/2170109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-[(1-tert-Butoxycarbonyl-cyclobutylmethyl)-sulfamoyl]-benzoic acid methyl esterHCID 66797535—
SolventTetrahydrofuranHCID 8028—
Product3-[(1-tert-Butoxycarbonyl-cyclobutylmethyl)-sulfamoyl]-benzoic acidHCID 66797532—

Reaction Steps

A solution of 3-[(1-tert-butoxycarbonyl-cyclobutylmethyl)-sulfamoyl]-benzoic acid methyl ester (step 3) (1.87 g, 4.88 mmol) in THF (25 ml) was treated with 2M NaOH (aq) (24.38 ml, 48.8 mmol) and stirred at RT for 2 h. The reaction mixture was partitioned between diethyl ether and water. The aqueous portion was separated and acidified to pH 1 with 2N HCl, and extracted with EtOAc, and the combined organic portions were washed with brine, dried over MgSO4 and concentrated in vacuo to afford the title product; 1H NMR (400 MHz, CDCl3) δ 8.64 (1H, s), 8.33 (1H, d), 8.12 (1H, d), 7.67 (1H, t), 5.40 (1H, t), 3.24 (2H, d), 2.38 (2H, m), 1.97 (4H, m), 1.48 (9H, s). LC-MS Rt 1.13 mins; 314.1 [M+H]+ (−tBu), Method 2minLC_v003.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050339B2
Source datasetuspto-grants-2015_06
ORD IDord-2a5e2a3f970f47b1a25984df3df2afd5
Source noteuspto-grants-2015_06