HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264329Generated: October 25, 2026
Heptane → methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate
https://huagongshe.com/reaction/264329
Participants
| Role | Name | HCID | Charge |
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| Reactant | Heptane | HCID 8900 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | N-[4-methoxybenzenesulfonyl]-(D)-valine | HCID 1133588 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate | HCID 10946547 | — |
Reaction Steps
To a solution of N-[4-methoxybenzenesulfonyl]-(D)-valine (8369 g, 29.13 mol) in methanol (30 L) at 5° C. is added thionyl chloride (2176 mL, 29.7 mol) over 2.5 hours. After stirring for 3 hours at 5° C., the reaction is stirred for 36 hours at room temperature. Most of the solvent is evaporated, and the crude product is dissolved in toluene (80 L). The toluene layer is then washed with water (20 L), saturated sodium bicarbonate (20 L), water again (20 L), 2N hydrochloric acid (20 L), brine (20 L), dried (Na2SO4), and the solvent is evaporated. The solid obtained is dissolved in ethyl acetate (8 L) and heptane (16 L) is added to induce crystallization. The precipitated product is collected by filtration to provide methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646167 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-ba04457198e54793b702012d62934ded |
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| Source note | uspto-grants-1997_07 |
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