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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880452Generated: October 31, 2026

Acetic Acid → HCID 86654671, compound

https://huagongshe.com/reaction/880452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86654670HCID 86654670—
SolventEthanolHCID 702—
ProductHCID 86654671HCID 8665467195%

Reaction Steps

2-(2-Formyl-4-iodo-pyrrol-1-yl)ethyl 4-methylbenzenesulfonate (2.1 g, 5.01 mmol) in ethanol (25 mL) was cooled to 0° C. and sodium borohydride (95 mg, 2.50 mmol) was added. After 30 min, the reaction mixture was allowed to warm to ambient temperature and stirred for a further 1 h, after which time acetic acid was added and the mixture was concentrated in vacuo. The residue was partitioned between water and dichloromethane and the organic phase was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give 2-[2-(hydroxymethyl)-4-iodo-pyrrol-1-yl]ethyl 4-methylbenzenesulfonate (2.0 g, 95%) as a brownish crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993574B2
Source datasetuspto-grants-2015_03
ORD IDord-dc18e67a3f4547c4b38589015a639fd7
Source noteuspto-grants-2015_03