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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647543Generated: October 31, 2026

Phenyl chloroformate → HCID 12694090, compound

https://huagongshe.com/reaction/647543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
ReactantHCID 12694071HCID 12694071—
SolventDichloromethaneHCID 6344—
ProductHCID 12694090HCID 12694090—

Reaction Steps

To 5.0 g of phenyl chloroformate in 80 ml of dichloromethane is added 7.89 g of the free base, 3-(3-fluorophenyl)-1,3-dihydro-1'-methylspiro[benzo(c)thiophene-1,4'-piperidine] of Example 55, in 10 ml of dichloromethane over 20 minutes. The reaction mixture is stirred at room temperature for 21 hours, then diluted with 200 ml of dichloromethane. The resultant mixture is washed with two 175 ml portions of 10% aqueous sodium hydroxide solution, two 150 ml portions of water and one 70 ml portion of saturated aqueous sodium chloride solution, and dried over magnesium sulfate to give an oil. The oil is chromatographed on silica gel with dichloromethane to give an oil, which crystallizes to yield 3-(3-fluorophenyl)-1,3-dihydro-1'-phenoxycarbonylspiro[benzo(c)thiophene-1,4'-piperidine], m.p. 134°-142° C. A portion is recrystallized twice from toluene:hexane, m.p. 144°-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409229
Source datasetuspto-grants-1983_10
ORD IDord-1a78b598fd4c4979b5159e292dc6f6b3
Source noteuspto-grants-1983_10