HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968532Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 69414918, compound
https://huagongshe.com/reaction/968532
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Methoxybenzyl alcohol | HCID 69154 | — |
| Reactant | (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid | HCID 69415969 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69414918 | HCID 69414918 | 75.1% |
Reaction Steps
0.200 g (0.6 mmol) of (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid, 0.138 g (1.0 mmol) of 2-methoxybenzyl alcohol, 0.088 g (0.33 mmol) of CAS, 0.227 g (1.2 mmol) of DCC and 0.04 g (0.33 mmol) of DMAP were dissolved in 15 mL of CH2Cl2. The mixture was stirred for 24 h at room temperature. The solid was filtrated and the solvent was evaporated. The residual was dissolved in a suitable amount of ethyl acetate (20 ml) and then the mixture was filtered to remove insoluble substance. The ethyl acetate was added to 60 ml and then the liquid was washed with 10% NaHCO3 solution, saturated NaCl solution and dried over Na2SO4. After the drying agent was removed and part of ethyl acetate was evaporated, the crude product was purified by flash column chromatography (eluent: ethyl acetate:cyclohexane=1:6) to obtain the product as a oil (0.19 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304057B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-8951efbfeb8c4fc4af6c73156fd0d253 |
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| Source note | uspto-grants-2007_12 |
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