HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277189Generated: October 25, 2026
Triethylamine → 3-[3-(1-Benzyloxycarbonylamino-3-methyl-butyl)-isoxazol-5-yl]-propionic acid methyl ester
https://huagongshe.com/reaction/277189
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-pentynoate | HCID 543061 | — |
| Reactant | [1-(Hydroxyimino-methyl)-3-methyl-butyl]-carbamic acid benzyl ester | HCID 73456130 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[3-(1-Benzyloxycarbonylamino-3-methyl-butyl)-isoxazol-5-yl]-propionic acid methyl ester | HCID 18682366 | 29.4% |
Reaction Steps
To a stirred solution of [1-(hydroxyimino-methyl)-3-methyl-butyl]-carbamic acid benzyl ester (6.0 g, 22.7 mmol) and pent-4-ynoic acid methyl ester (3.8 g, 34 mmol) in CH2Cl2 (80 ml) was added triethylamine (0.2 ml) followed by Clorox bleach (80 ml). After 4 h at room temperature the organic phase was separated and the aqueous phase was extracted with CH2Cl2 (25 ml×3). The combined organics were dried over MgSO4; filtered and concentrated under reduced pressure to give a yellow oil. Purification by Flash 40 chromatography using a silica gel column and eluting with 10-20% EtOAc/hexane gave 2.5 g of the title compound as a waxy pale yellow solid. MS [M+1]+375.3; 1H nmr (400 MHz, CDCl3) δ0.91 (m, 6H), 1.51-1.76 (m, 3H), 2.67 (t, J=7.5 Hz, 2H), 3.02 (t, J=7.5 Hz, 2H), 3.67 (s, 3H), 4.89 (m,1H), 5.08 (m, 3H), 5.92 (s, 1H), 7.31 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355662B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-fa3c518b4c5e4061b286a9d6731fa3fc |
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| Source note | uspto-grants-2002_03 |
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