HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156952Generated: October 31, 2026
Tetrahydrofuran → Ethyl (tert-butoxycarbonyl)-D-methionylglycinate
https://huagongshe.com/reaction/1156952
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione | HCID 89529 | — |
| Reactant | N-(tert-Butyloxycarbonyl)-D-methionine | HCID 111051 | — |
| Product | Ethyl (tert-butoxycarbonyl)-D-methionylglycinate | HCID 12919642 | — |
Reaction Steps
In 100 ml of THF are dissolved 10.0 g of BOC-(D)-Met-OH and 7.9 g of HONB, followed by cooling at 0° C. and adding 9.0 g of DCC, and the mixture is stirred at 0° C. for 6 hours. Insoluble matters are filtered out, and 5.9 g of H-Gly-OEt.HCl salt and 5.6 ml of TEA are added to the filtrate, which is then stirred overnight at room temperature. The THF is distilled off and the residue is extracted with 100 ml of AcOEt, followed by washing with water and drying over anhydrous sodium sulfate. The AcOEt is distilled off and the residue is crystallized with petroleum ether. Recrystallization from AcOEt-petroleum ether yields 9.8 g of the desired product, m.p. 55°-56° C., Rf1 =0.70, [α]D21 +12.5° (c=0.67, DMF).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04337247 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-0bca650f6b8d44deb938267694ab8697 |
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| Source note | uspto-grants-1982_06 |
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