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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018686Generated: October 27, 2026

Water → 1-(N-(4-hydroxybutyl)pentafluorophenylsulfonamido)-4-methoxybenzene

https://huagongshe.com/reaction/1018686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium PerborateHCID 517072—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantHCID 21884144HCID 21884144—
SolventTetrahydrofuranHCID 8028—
Product1-(N-(4-hydroxybutyl)pentafluorophenylsulfonamido)-4-methoxybenzeneHCID 2188411964%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-(N-(3-butenyl)pentafluorophenylsulfonamido)-4-methoxybenzene (410 mg, 1.01 mmol) in THF (6.5 mL) at −78° C. was added BH3.THF (1.00 mL of a 1 M solution in THF, 1.00 mmol). After stirring at −78° C. for 1 h and at 0° C. for 1 h, the reaction mixture was treated with H2O (20 mL) and sodium perborate (513 mg, 5.14 mmol). After stirring at rt for 2 h, the mixture was poured onto H2O (20 mL) and extracted with CH2Cl2 (3×15 mL). The combined organic extracts were washed with sat. NaCl (20 mL) and dried (MgSO4). Concentration followed by chromatography (2:1/hexanes:EtOAc) afforded 270 mg (64%) of product as a white solid, mp 88-90° C. 1H NMR (CDCl3): d 7.08 (m, 2H), 6.85 (m, 2H), 3.80 (s, 3H), 3.77 (m, 2H), 3.64 (t, J=6.0; 2H), 1.63-1.55 (m, 5H), 1.50 (bs, 1H). Anal. Calcd. for C17H16F5NO4S: C, 48.00; H, 3.79; N, 3.29; S, 7.54. Found: C, 48.08; H, 3.76; N, 3.34; S, 7.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482860B1
Source datasetuspto-grants-2002_11
ORD IDord-986797f2818e4e7985db74d1da79c866
Source noteuspto-grants-2002_11