HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592007Generated: October 29, 2026
Triphenylphosphine → HCID 67139934, compound
https://huagongshe.com/reaction/1592007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Benzyl 4-(hydroxymethyl)benzoate | HCID 15650225 | — |
| Reactant | HCID 66751042 | HCID 66751042 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67139934 | HCID 67139934 | — |
Reaction Steps
To a solution of the title B compound in Example 9, 2-(2,4-dimethoxybenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (2.0 g, 7.0 mmol) and 4-hydroxymethyl-benzoic acid benzyl ester (2.54 g, 10.5 mmol) in THF (50 mL) is added triphenylphosphine (3.67 g, 14 mmol) and the mixture is stirred until dissolved. The reaction is cooled to 0° C. and diethyl azodicarboxylate (2.20 mL, 14 mmol) dissolved in THF (20 mL) is added dropwise. The reaction is stirred for 16 h, while allowing to warm to RT, then concentrated. The residue is taken up in CH2Cl2, and chromatographed in two portions on a 110 g silica gel RediSep column (Isco, Inc.) with a 30 mL/min gradient elution of 0:100 (EtOAc:hexane) to 5:95 over 10 min. Fractions containing product are combined and concentrated to yield 4-[5-(2,4-dimethoxy-benzyl)-1,1,4-trioxo-1,2,5-thiadiazolidin-2-ylmethyl]-benzoic acid benzyl ester as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07291635B2 |
|---|
| Source dataset | uspto-grants-2007_11 |
|---|
| ORD ID | ord-5a3ce1d0c0bc44dbba17bf51d08304c9 |
|---|
| Source note | uspto-grants-2007_11 |
|---|