HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424981Generated: October 30, 2026
Tetrahydrofuran → HCID 66703639, compound
https://huagongshe.com/reaction/424981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86622774 | HCID 86622774 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66703639 | HCID 66703639 | — |
Reaction Steps
To a stirred solution of (R)-1-(2,5-difluorophenylmethyl)-3-chloro-2-oxopropylcarbamic acid tert-butyl ester (3.56 g, 11 mmol) in a solution of 9:1 THF:water (150 mL) at 0° C. is added NaBH4 (0.49 g, 13 mmol, 1.2 eq) and stirred for 5 min. The reaction mixture is concentrated under reduced pressure to a white solid which is suspended in a mixture of water and ethyl acetate. This biphasic mixture is cooled to 0° C. and quenched slowly with 2M NaHSO4 until pH˜2 and the layers rapidly separated. The organic layer is washed with water and brine, dried over Na2SO4 and concentrated under reduced pressure to afford a white solid as a mixture of diastereomers (3.5 g, 13 mmol, ˜5:2 R,R:R,S). The crude material was purified using General Purification Procedure C to afford the title compound as a single diastereomer of a white solid (2.2 g, 6.6 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106090B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-a3b330f3e9ea4ad7b6eff2fbb97b6aab |
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| Source note | uspto-grants-2012_01 |
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