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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722548Generated: October 25, 2026

Phenanthro[1,2-b]furan-2-methanol → Phenanthro[1,2-b]thiophene-2-methanol

https://huagongshe.com/reaction/1722548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenanthro[1,2-b]furan-2-methanolHCID 14770239—
ReactantEthyl phenanthro[1,2-b]thiophene-2-carboxylateHCID 14770247—
SolventMethylenechloride HexaneHCID 21226440—
ProductPhenanthro[1,2-b]thiophene-2-methanolHCID 1477024898%

Reaction Steps

Using the procedure outlined in 14A, ethyl phenanthro[1,2-b]thiophene-2-carboxylate (H. G. Pars Pharmaceutical Laboratories, Inc.) gave a 98.0% yield of phenanthro[1,2-b]thiophene-2-methanol, mp 169°-170.5° (C,H,S), (CH2Cl2 /hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855453
Source datasetuspto-grants-1989_08
ORD IDord-2039e7cae5e644a18ff551ce64db4f17
Source noteuspto-grants-1989_08