Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680015Generated: November 2, 2026

Phosphoric Acid → HCID 23458724, compound

https://huagongshe.com/reaction/1680015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHCID 70574841HCID 70574841—
SolventDichloromethaneHCID 6344—
ProductHCID 23458724HCID 23458724—

Reaction Conditions

Temperature-20 °C

Reaction Steps

9.1 g (0.0177 mole) of alpha-amino-4-benzyloxycarbonyl-8-phenyl-1-thia-3,8-diazaspiro[4.5]decane-2-acetic acid dihydrochloride (obtained in 5.3) are suspended in 150 ml of dichloromethane. After cooling to -20° C., 18,6 g (0.0668 mole) of trityl chloride are added all at once. While maintaining the temperature at about -20° C., the suspension is slowly treated over the course of 1 hour with 17.6 g (0.17 mole) of triethylamine in 100 ml of dichloromethane. The reaction mixture is stirred for 1 hour at a temperature of from -10 to -20° C. and then left to stand overnight in a refrigerator, whereafter it is poured onto an ice-water mixture (pH about 11) and neutralized to about pH 6 by the addition of 85% phosphoric acid. The aqueous phase is extracted three times with 100 ml of dichloromethane. The combined extracts are washed with water and dried over anhydrous sodium sulfate, followed by evaporation to dryness under high vacuum on a waterbath at a temperature of from 20° to 25° C. The 4-benzyloxycarbonyl-8-phenyl-alpha-tritylamino-1-thia-3,8-diazaspiro[4.5]-decane-2-acetic acid thus obtained is used, without further purification, in step 7.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04271172
Source datasetuspto-grants-1981_06
ORD IDord-14c814a31ab34488aa6363d413158fe8
Source noteuspto-grants-1981_06