HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57752Generated: October 26, 2026
Diethyl 2-t-butyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate → (R)-1-benzyl hydrogen 3-t-butyloxycarbonylamino-3-ethoxycarbonylsuccinate
https://huagongshe.com/reaction/57752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl 2-t-butyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate | HCID 66725227 | — |
| Solvent | Phosphate | HCID 1061 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (R)-1-benzyl hydrogen 3-t-butyloxycarbonylamino-3-ethoxycarbonylsuccinate | HCID 66725181 | — |
Reaction Steps
1.0 g of pig liver esterase produced by Sigma [PLE (27 kU/g), lyophilized product, product number: E3019] was dissolved in a 0.1 mol/L phosphate buffer adjusted to pH 7.5 (90 mL), and the solution was added with a solution of diethyl 2-t-butyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate (1.0 g) dissolved in acetonitrile (10 mL). The mixture was stirred at 30° C. for 4 hours to produce the title compound. Optical purity measured by HPLC was 78.1% ee. After completion of the reaction, the reaction mixture was filtered by using a filtration aid (KC Floc 100) to remove the insoluble matter. The filtrate was cooled, and adjusted to pH 2 by adding 6 mol/L hydrochloric acid, then the objective substance was extracted with ethyl acetate, and the extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain the title compound (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434737B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-97e63dce37f24e41bd0669010e1bb380 |
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| Source note | uspto-grants-2016_09 |
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