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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021335Generated: October 31, 2026

Hydrochloric Acid → 6-Chloro-7-hydroxychroman-4-carboxylic acid

https://huagongshe.com/reaction/1021335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropyl AcetateHCID 7915—
ReactantStannous chloride dihydrateHCID 61436—
Reactant6-Chloro-4,7-bis(trimethylsilyloxy)chroman-4-carbonitrileHCID 67080315—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product6-Chloro-7-hydroxychroman-4-carboxylic acidHCID 67080428125.2%

Reaction Steps

A 20-liter 4-neck round-bottom flask was charged with glacial acetic acid (2.04 L), 6-chloro-4,7-bis(trimethylsilyloxy)chroman-4-carbonitrile (2.2 kg, 5.94 mol), and tin(II) chloride dihydrate (3.35 kg, 14.85 mol) and the resulting mixture was stirred at ambient temperature. Concentrated hydrochloric acid (5.0 L, 60 mol) was added, and the resulting mixture was stirred and heated to 80-85° C. for 12 hours. The reaction mixture was cooled to ambient temperature and water (3.6 L) was added, and stirring was continued at ambient temperature for 15 minutes. Isopropyl acetate (11.5 L) and water (5.8 L) were added, and stirring was continued at ambient temperature for 15 minutes. The layers were separated, and the aqueous layer was extracted with isopropyl acetate (2×2 L). The organic layers were combined and washed with brine (3×6 L), then dried over sodium sulfate and concentrated under reduced pressure at a temperature below 50° C. to afford crude 6-chloro-7-hydroxychroman-4-carboxylic acid as a brown semi-solid (1.70 kg, 125% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-94ced5ac04c540efadb0c0ec6cc1c29b
Source noteuspto-grants-2014_05