HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164137Generated: October 31, 2026
Chlorobenzene → 5-Chloro-3-methyl-2-phenyl-1-benzothiophene
https://huagongshe.com/reaction/2164137
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | p-Chlorophenylthiophenylmethylmethyl ketone | HCID 131711410 | — |
| Product | 5-Chloro-3-methyl-2-phenyl-1-benzothiophene | HCID 821982 | — |
Reaction Steps
55.7 parts by weight of p-chlorophenylthiophenylmethylmethyl ketone and 500 parts by weight polyphosphoric acid are combined in a stoppered flask and heated with stirring for 3.5 hours at 180° C. 350 Parts by volume of chlorobenzene is added to the reaction mixture and the resulting solution is heated at reflux temperature for an additional hour. After cooling the organic phase of this reaction solution is decanted off; the inorganic phase is dissolved in ice water and extracted once each with benzene and ethyl ether. The combined organic phases are then washed once with a saturated solution of sodium bicarbonate, washed once with brine, and dried over magnesium sulfate. Concentration of this solution in vacuo affords a dark solid. Crystallization of this solid (2xs) from heptane affords a brown solid. Sublimation at 135° C/0.1mm of this brown solid affords 5-chloro-3-methyl-2-phenylbenzo[b]thiophene, melting at 108.5°-110° C. This compound is represented by the following structural formula. ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04137414 |
|---|
| Source dataset | uspto-grants-1979_01 |
|---|
| ORD ID | ord-df083cc5f7484a98a2c3a1fad5bd9e7c |
|---|
| Source note | uspto-grants-1979_01 |
|---|