HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276365Generated: October 29, 2026
Chlorotrimethylsilane → HCID 55282880, compound
https://huagongshe.com/reaction/2276365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 55282881 | HCID 55282881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 55282880 | HCID 55282880 | 28% |
Reaction Steps
To a stirred solution of lithium borohydride in THF (48.9 ml, 2 M solution) under an argon atmosphere was added dropwise chlorotrimethylsilane (25.0 ml). The resulting suspension was cooled to 0° C. and (RS)-amino-(3-fluoro-2-methyl-phenyl)-acetic acid (7.1 g) was added portionwise, whereby the temperature of the reaction mixture rose transiently to 45° C. The ice bath was removed and stirring was then continued at r.t. for 90 min. The mixture was quenched by dropwise addition of methanol (20 ml) and then concentrated in vacuo. The residue was suspended in ethyl acetate and washed with 2 N aq NaOH. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated in vacuo to afford (RS)-2-amino-2-(3-fluoro-2-methyl-phenyl)-ethanol (1.83 g, 28%) as a light yellow solid. MS (ISP): 170.3 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09132136B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-0f0303980deb4ae4818c6efecc290540 |
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| Source note | uspto-grants-2015_09 |
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