HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860092Generated: November 2, 2026
Dimethyl methylphosphonate → (7-tert-Butoxycarbonylamino-2-oxo-heptyl)-phosphonic acid dimethyl ester
https://huagongshe.com/reaction/860092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Boc-6-Ahx-OSu | HCID 5074016 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7-tert-Butoxycarbonylamino-2-oxo-heptyl)-phosphonic acid dimethyl ester | HCID 20622500 | 105.8% |
Reaction Steps
A solution of dimethyl methylphosphonate (9.308 g, 75.01 mmol) in THF (30 mL) was cooled to −78 ° C. and treated with n-butyllithium (29.5 mL of 2.5 M). The reaction mixture was stirred at −78 ° C. for 10 min, followed by addition of 6-tert-butoxycarbonylamino-hexanoic acid 2,5-dioxo-pyrrolidin-1-yl ester (24-1) (5.060 g, 15.41 mmol) in THF (30 mL). After 15 min the reaction was quenched with aqueous NH4Cl and allowed to warm to room temperature overnight. The water was extracted three times with ethyl acetate and the combined organics washed with brine and dried (Na2SO4). The solvent was removed in vacuo to afford the title compound 24-2 as a pale yellow oil (5.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153862B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-632d255c771449be809672fa3420dff6 |
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| Source note | uspto-grants-2006_12 |
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