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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352644Generated: October 30, 2026

Iodine → Benzoic acid, 3-mercapto-

https://huagongshe.com/reaction/352644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantSodium ChlorideHCID 5234—
ReactantBenzoic acid, 3-(chlorosulfonyl)-HCID 77641—
CatalystIodineHCID 807—
SolventAcetic AcidHCID 176—
ProductBenzoic acid, 3-mercapto-HCID 9573792%

Reaction Conditions

Temperature110 °C

Reaction Steps

3-Chlorosulfonylbenzoic acid (156.0 g, 0.707 mol), acetic acid (240 mL), and red phosphorus (78.5 g, 2.53 mol) were placed in a 2-L three-neck flask. The mixture was heated to 110° C. and stirred while a solution of iodine (2.82 g, 0.011 mol) in acetic acid (66 mL) was added dropwise over about 30 min, so as to maintain the color of iodine vapor. The stirred mixture was cooled to 100° C. and treated dropwise with 41 mL (2.3 mol) of water over a 10-min period, then heated at reflux temperature for 1.5 h and subsequently cooled to 90° C. Following the addition of saturated sodium chloride solution (250 mL) and water (500 mL), the mixture was kept at 0-5° C. for 1 h and filtered. The damp filter cake was slurried with 450 mL of acetone, and the excess red phosphorus was removed by filtration; then the acetone was evaporated from the filtrate while adding 500 mL of water. The resultant solid was filtered off and dried under vacuum to give 100.1 g (92%) of 3-mercaptobenzoic acid, mp 138-141° C. (lit. mp 138-141° C.); 1H NMR (400 MHz, in CDCl3 w/TMS, ppm) 3.59 (s, SH), 7.36 (t, J=7.8 Hz, H-5), 7.51 and 7.90 (2d, J=7.8 Hz, H-4 and H-6), 8.03 (s, H-2); {1H}13C NMR (100 MHz, in CDCl3 w/TMS, ppm) 171.77 (C═O), 134.49 (C-4), 132.24 (C-1), 130.86 (C-2), 130.34 (C-3), 129.42 (C-5), 127.59 (C-6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747081B2
Source datasetuspto-grants-2004_06
ORD IDord-ea35cf69eece4686a0f933f2a9cf9ac2
Source noteuspto-grants-2004_06