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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529197Generated: November 1, 2026

Hydrochloric Acid → 6-Propoxy-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

https://huagongshe.com/reaction/529197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-BromopropaneHCID 7840—
ReactantSodium hydrideHCID 24758—
Reactant1,3-Dihydro-2,1-benzoxaborole-1,6-diolHCID 52919291—
SolventDimethylformamideHCID 6228—
Product6-Propoxy-1,3-dihydro-1-hydroxy-2,1-benzoxaboroleHCID 5135126764%

Reaction Conditions

Temperature0 °C

Reaction Steps

H181 (110 mg, 0.73 mmol) was dissolved in DMF (6.0 mL) and cooled to 0° C. with ice bath. To this solution under nitrogen were added in sequence NaH (60% in mineral oil, 117 mg, 2.93 mmol) and 1-bromopropane (0.26 mL, 2.93 mmol). The reaction mixture was stirred for 1 d then treated with 1.0 M HCl (10.0 mL). After extraction with ethyl acetate, the organic phase was washed with water and brine, and dried over anhydrous Na2SO4. The residue after rotary evaporation was purified by column chromatography over silica gel to give the title compound (89 mg, 64% yield). 1H NMR (400 MHz, DMSO-d6): δ 9.10 (s, 1H), 7.29 (d, J=8.4 Hz, 1H), 7.23 (d, J=2.4 Hz, 1H), 7.03 (dd, J=8.1 & 2.4 Hz, 1H), 4.91 (s, 2H), 3.92 (t, J=6.8 Hz, 2H), 1.78-1.68 (m, 2H) and 0.98 (t, J=7.2 Hz, 3H) ppm; Mp: 80-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346834B2
Source datasetuspto-grants-2016_05
ORD IDord-322754b800fb4806b6af2a940ace7bf3
Source noteuspto-grants-2016_05