HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971861Generated: November 4, 2026
4-Methylmorpholine → HCID 66688142, compound
https://huagongshe.com/reaction/1971861
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Boc-D-phenylalanine | HCID 637610 | — |
| Reactant | HCID 22313260 | HCID 22313260 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66688142 | HCID 66688142 | 87% |
Reaction Steps
A solution consisting of 10 g of Boc-D-Phe-OH, 40 ml of tetrahydrofuran and 4.6 ml of N-methylmorpholine is slowly dripped into a solution of 5.4 ml of isobutyl chloroformate in 60 ml of tetrahydrofuran cooled to 0° C., at a rate such that the inner temperature does not exceed 5° C. The resulting mixture is maintained under stirring at 0° C. for 0.5 hours. A solution consisting of 8.0 g of (11) in 20 ml of tetrahydrofuran is then dripped into the reaction mixture at a rate such that the temperature does not exceed 5° C. The solution is maintained under stirring at 0° C. for 1 hour, and at ambient temperature for 5 hours. 100 ml of 1M NaOH is added to the mixture, and the tetrahydrofuran is evaporated at low pressure. The residue is taken up with dichloromethane and water; the organic phase is washed with water (2×), and after a solvent change with ethyl acetate at low pressure, compound (12) is crystallised from ethyl acetate to obtain 15 g of white solid. Yield 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431684B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-b3a4b736666743f3a8eb8908d1c158e0 |
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| Source note | uspto-grants-2013_04 |
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